10172-75-5

  • Product Name:Coumarin
  • Molecular Formula:C26H18 O7
  • Molecular Weight:442.425
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Product Details

Purity:99%

Factory sells Coumarin 10172-75-5 with sufficient production capacity

  • Molecular Formula:C26H18 O7
  • Molecular Weight:442.425
  • Boiling Point:632.6°Cat760mmHg 
  • Flash Point:218.5°C 
  • PSA:110.11000 
  • Density:1.495g/cm3 
  • LogP:4.49940 

10172-75-5 Relevant articles

Synthesis of biscoumarin and dihydropyran derivatives as two novel classes of potential anti-bacterial derivatives

Li, Jing,Xue, Xiao-yan,Li, Xia,Hou, Zheng,Yang, Xiao-hui,Qu, Di,Zhou, Ying,Zhang, Zi-dan,Luo, Xiao-xing,Li, Jiang-tao,Li, Ming-kai

, p. 1349 - 1355 (2016)

A series of bisoumarin (1–4) and dihydro...

Aldehyde condensation products of 4-hydroxycoumarin and Schiff bases

Manolov, Ilia I.

, p. 3041 - 3042 (1998)

4-Hydroxycoumarin and Schiff bases conde...

Impact of solvents on energy gap, photophysical, photometric properties for a new class of 4-HCM coumarin derivative: Nonlinear optical studies and optoelectronic applications

Pramod,Renuka,Nadaf,Rajaramakrishna

, (2019)

Now a day the derivatives of biscoumarin...

Synthesis of unexpected novel bis-coumarin derivatives via three component reactions of 4-hydroxycoumarin, aldehydes and cyclic secondary amines. Conformation in the solid state and pharmacological evaluation

El-Samahy, Fatma A.,Abd El Salam, Hayam A.,El-Sayed, Naglaa F.,Shalaby, Elsayed M.,Dondeti, Mahmoud F.

, p. 705 - 716 (2017)

A series of unexpected bis-coumarins hav...

Synthesis, photophysical properties, chemo-sensing ability and computational studies of biscoumarin derivatives

Harichandran, G.,Nehru, S.,Surya, C. P.

, (2021/09/20)

Synthesis of biscoumarin derivatives usi...

Facile and Straightforward Synthesis of Racemic Version of Substituted 3-[3-(2-Hydroxyphenyl)-3-oxo-1-arylpropyl]-4-hydroxycoumarins: Easy Access to a Series of Biorelevant Warfarin Analogues

Brahmachari, Goutam,Mandal, Mullicka,Karmakar, Indrajit

, p. 451 - 464 (2021/10/19)

The present communication deals with a s...

Chitosan and functionalized graphene oxide nanocomposite as a novel and highly efficient catalyst for production of bis-coumarins under solvent-free conditions

Atashrouz, Zhale,Rostami, Esmael,Zare, Abdolkarim

, p. 179 - 201 (2021/11/18)

Chitosan and functionalized graphene oxi...

Developing a highly potent anthelmintic: study of catalytic application of l-proline derived aminothiourea in rapid synthesis of biscoumarins and their in vitro anthelmintic essay

Kharrngi, Balamphrang,Dhar, Errini Decruse,Basumatary, Grace,Das, Dharitri,Deka, Ramesh Ch,Yadav, Arun K,Bez, Ghanashyam

, (2021/02/22)

Abstract: Due to serious side effects of...

10172-75-5 Process route

4‐hydroxycoumarin
22105-09-5

4‐hydroxycoumarin

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

3,3-(4'-methoxybenzylidene)bis(4-hydroxycoumarin)
10172-75-5

3,3-(4'-methoxybenzylidene)bis(4-hydroxycoumarin)

Conditions
Conditions Yield
With Ni(II)-dimethylglyoxime complex immobilized on SiO2 coated magnetic Fe3O4 nanoparticles; In water; for 0.05h; Reflux; Green chemistry;
98%
With acetic acid; for 3h; Reflux;
92%
With Zn-Ni-Fe layered double hydroxide on Fe3O4-graphene oxide nanocomposite; In water; for 0.333333h; Reflux; Green chemistry;
91%
With Ni(0) nanoparticles anchored on micro/mesoporous acid-activated montmorillonite; In ethanol; for 0.0833333h; Microwave irradiation;
90%
With magnetite nanoparticles-supported boron hydrogen sulfate; In neat (no solvent); at 80 ℃; for 0.166667h;
90%
With ChitosanGOAM-SO3H nanocomposite; at 80 ℃; for 0.333333h;
88%
With iron(III) chloride hexahydrate; sodium dodecyl-sulfate; In water; at 100 ℃; for 0.5h; Green chemistry;
68%
4-hydroxy[1]benzopyran-2-one
1076-38-6,92395-12-5

4-hydroxy[1]benzopyran-2-one

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

3,3-(4'-methoxybenzylidene)bis(4-hydroxycoumarin)
10172-75-5

3,3-(4'-methoxybenzylidene)bis(4-hydroxycoumarin)

Conditions
Conditions Yield
With 4-sulfophthalic acid; In water; at 80 ℃; for 0.416667h; Catalytic behavior; Green chemistry;
100%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; at 20 ℃; for 16h;
99%
With phosphotungstic acid; In water; at 80 ℃; for 0.383333h;
99%
With Sulfonic Acid Functionalized Nanoporous Silica (SBA-Pr-SO3H); In ethanol; water; for 0.5h;
99%
With piperidine; In ethanol; at 20 ℃; for 4h;
98%
With bismuth(III) vanadate; In water; at 80 ℃; for 1.5h;
98%
With 1,4-diazabicyclo[2.2.2]octane hydroacetate; In water; at 80 ℃; for 0.05h; Green chemistry;
98%
With polystyrene functionalized zinc anthranilic acid complex; In water; at 100 ℃; for 0.05h; Reagent/catalyst; Solvent; Catalytic behavior;
98%
With Zn(II)-grafted benzene-benzylamine-imine-based porous organic polymer; In water; at 80 ℃; for 0.0333333h; Catalytic behavior; Green chemistry;
98.5%
In toluene; at 90 ℃; for 0.333333h; Reagent/catalyst;
97%
With C19H40KNO8S(2+)*2C2F3O2(1-); In ethanol; water; for 0.5h; Reflux;
96%
With poly(2-acrylamido-2-methylpropanesulphonic acid-co-acrylamide) supported on magnetite nanoparticles; In toluene; at 90 ℃; for 0.333333h;
96%
With diammonium iron(II) sulfate hexahydrate; In water; for 0.416667h; Reflux; Green chemistry;
95%
With cholin hydroxide; In water; at 50 ℃; for 1h;
95%
With 2-(3-phenylthioureido)ethylprolinamide; In water; for 0.25h; Reflux;
95%
With lemon juice; In water; at 27 - 30 ℃; for 2h;
95%
In water; at 95 ℃; for 5h; Solvent; Time;
94%
With Triton X-100; In water; at 20 ℃; for 7h; Green chemistry;
94%
With Mn(2,2’-bipyridine-1,1’-dioxide)2Cl2/Mobil Composition of Matter No. 41; In water; for 0.666667h; Reflux; Green chemistry;
94%
With bael fruit ash; In water; at 20 ℃; for 0.25h; Reagent/catalyst; Solvent; Temperature; Green chemistry;
94%
With 1-ethyl-3-(3-sulfopropyl)-benzimidazolium trifluoromethanesulfonate; at 70 ℃; for 2.5h;
93%
With 30C2H3O2(1-)*72H2O*42H3N*42H(1+)*72Mo(6+)*60Mo(5+)*372O(2-); In ethanol; for 0.133333h; Reflux;
93%
With C5H9NO*Cl3Zn(1-)*H(1+); In neat (no solvent); at 100 ℃; for 0.666667h; Green chemistry;
93%
With nanoparticles of the immobilized Ni(II) species on thiourea functionalized copper ferrite (CuFe2O4SiO2PTMSTuNi(II)); In neat (no solvent); at 70 ℃; for 0.333333h;
93%
With SO3H at Fe3O4 magnetic nanoparticles; In neat (no solvent); at 80 ℃; for 0.166667h;
93%
With carbon-SO3H; In ethanol; water; at 80 ℃; for 0.25h; Green chemistry;
93%
With aluminized polyborate; In neat (no solvent); at 90 ℃; for 0.583333h; Green chemistry;
93%
With rhodium(III) chloride hydrate; In water; at 80 ℃; for 0.5h;
92%
With sulfated titania; In water; at 80 ℃; for 0.2h;
92%
With sulfonated rice husk ash; In water; at 80 ℃; for 0.25h; Green chemistry;
92%
With poly(4-vinylpyridine-co-1-sulfonic acid butyl-4-vinylpyridinium)chloroaluminate; In toluene; at 90 ℃; for 0.8h;
92%
With Amberlite IRA-400 Cl resin; In ethanol; water; at 80 ℃; for 2h;
92%
With poly(4-vinylpyridine-co-1-sulfonic acid butyl-4-vinylpyridinium)hydrogen sulfate; In toluene; at 90 ℃; for 1h;
91%
With C2H8NO7S2(1+)*HO4S(1-); In ethanol; for 0.466667h; Reflux;
91%
With silica-supported Preyssler acid nanoparticles; In ethanol; at 25 ℃; for 0.416667h;
90%
With L-tyrosine loaded polymeric nanoparticles; In water; at 70 ℃; for 0.0833333h; Reagent/catalyst; Solvent; Catalytic behavior; Green chemistry;
90%
With graphene oxide nanosheets; In water; for 0.3h; Reflux; Green chemistry;
90%
With V2O5 based quadruple strontium titanate nanoparticles; for 0.416667h;
90%
With magnetic nanostructured natural hydroxyapatite; In neat (no solvent); at 90 ℃; for 1.16667h; Green chemistry;
90%
With proton exchanged montmorillonite K10; In ethanol; water; at 20 ℃; for 0.583333h;
90%
With CuFe2O4(at)SiO2(at)3-(2-aminoethylamino)propyl trimethoxysilane(at)Ni(II)nanocomposite; In water; for 0.533333h; Reagent/catalyst; Reflux; Green chemistry;
90%
With 4-aminobenzene sulfonic acid; In water; at 80 ℃; for 0.416667h; Green chemistry;
90%
With Lipase B Candida Antarctica immobilized on immobead 150 recombinant from yeast; In ethanol; at 20 ℃; for 9h; Green chemistry;
90%
at 80 ℃; for 0.5h; Neat (no solvent); Ionic liquid;
89%
With poly(4-vinylpyrridine) supported copper(II) oxide nanoparticles; In water; for 0.583333h; Reflux;
89%
With 1H-imidazole; In neat (no solvent); at 60 ℃; for 0.416667h; Reagent/catalyst;
89%
In ethanol; at 20 ℃; for 2h; Irradiation; Green chemistry;
89%
With Thiamine hydrochloride; In neat (no solvent); at 20 ℃; Green chemistry;
89%
With KF/montmorillonite clay; In N,N-dimethyl-formamide; at 80 ℃;
88%
With bis(tetrabutylammonium) hexatungstate; In ethanol; for 0.0833333h; Reflux;
88%
With methanesulfonic acid; In ethanol; at 120 ℃; for 0.133333h; Microwave irradiation;
88%
With o-benzenedisulfonimide; In water; for 0.416667h; Reflux;
88%
With caffeine, phosphoric acid; In neat (no solvent); at 80 ℃; for 1.08333h; Green chemistry;
88%
With bis(ethylferrocene) modified imidazolium hydrogenoxalate supported on silica coated nanomagnetic Fe3O4; In ethanol; Reflux;
88%
With 1-butyl-3-methylimidazolium o-sulfonbenzimide; In water; at 80 ℃; for 0.416667h;
88%
With 1-butyl-3-methylimidazolium Tetrafluoroborate; at 60 - 70 ℃; for 3h;
87%
With sodium docusate; In water; at 60 ℃; for 0.116667h; Microwave irradiation;
87%
With triethylamine sulfate; In ethanol; at 80 ℃; for 0.5h;
87%
With acetic acid functionalized poly(4-vinylpyridinum)bromide; In neat (no solvent); at 70 ℃; for 0.3h; Green chemistry;
87%
With indium(III) chloride; In water; at 110 ℃; for 0.333333h; Microwave irradiation; Green chemistry;
87%
With sulfosalicylic acid functionalized Fe3O4 nanoparticle; In water; at 60 ℃; for 0.233333h; Microwave irradiation;
87%
With ammonium cerium (IV) nitrate; In water; Irradiation;
87%
With silica gel; for 0.116667h; microwave irradiation;
86%
With fermented bakers’ yeast; In aq. phosphate buffer; at 20 ℃; for 0.4h; Green chemistry;
86%
With N,N,N',N'-tetramethylguanidinium acetate; at 25 ℃; for 4.5h;
86%
With lipase from porcine pancreas; In ethanol; at 45 ℃; for 4h; Enzymatic reaction;
86%
With ethylenediamine diacetic acid; In ethanol; for 96h; Ambient temperature;
85%
With propane-1,2,3-triyl tris(hydrogen sulfate); In water; at 80 ℃; for 0.166667h; Solvent; Green chemistry;
85%
With Starch-sulfuric acid; In neat (no solvent); at 80 ℃; for 0.133333h;
85%
With sulfonic acid-functionalized mesoporous silica nanoparticles; In water; at 80 ℃; for 0.5h; Green chemistry;
85%
With silica-bonded 1,4-diaza-bicyclo[2.2.2]octanesulfonic acid chloride nanostructure; In neat (no solvent); at 70 ℃; for 0.283333h;
85%
With tetrabutylammomium bromide; In water; at 100 ℃; for 0.5h;
84%
With titanium(IV) oxide; In water; for 0.0833333h; Reflux;
84%
With copper chromite nanoparticles; In water; at 20 ℃; for 0.05h; Green chemistry;
84%
With boron tri(hydrogen sulphate); In ethanol; water; at 70 ℃; for 0.0833333h;
83%
In water; at 100 ℃; Green chemistry;
82%
In ethanol; for 24h; Reflux;
80%
With magnetite encapsulated hot-water soluble starch nanoparticles; In water; at 90 ℃; for 0.716667h; Green chemistry;
80%
With 1,8-diazabicyclo[5.4.0]undec-7-ene functionalized cellulose nanofibers; In water; at 25 ℃; for 3h; Green chemistry;
80%
In ethanol; for 0.05h; Heating;
79%
In ethanol; for 5h; Heating;
78%
With 1-n-butyl-3-methylimidazolim bromide; at 60 ℃; for 0.666667h;
78%
In water; at 150 ℃; for 0.133333h; Microwave irradiation;
76%
With magnesia; In neat (no solvent); at 100 ℃; for 0.466667h; Green chemistry;
76%
With piperidine; at 90 ℃;
66%
With ethanol;
With acetic acid;
In acetic acid; Heating;
With hydrogenchloride; In ethanol; water; Reflux;
With titania sulfonic acid; In water; at 80 ℃; for 0.666667h;
With piperidine; In ethanol; at 20 ℃; for 3h;
With piperidine; In ethanol; at 20 ℃; for 3h;

10172-75-5 Upstream products

  • 1076-38-6
    1076-38-6

    4-hydroxy[1]benzopyran-2-one

  • 123-11-5
    123-11-5

    4-methoxy-benzaldehyde

  • 836-41-9
    836-41-9

    p-methoxybenzylidene-phenylamine

  • 68029-57-2
    68029-57-2

    2-cyano-3-(4-methoxyphenyl)thioacrylamide

10172-75-5 Downstream products

  • 93322-00-0
    93322-00-0

    4-hydroxy-3-<(4-methoxyphenyl)methyl>-2H-1-benzopyran-2-one

Relevant Products