4651-91-6

  • Product Name:2-AMINO-4,5,6,7-TETRAHYDRO-1-BENZOTHIOPHENE-3-CARBONITRILE
  • Molecular Formula:C9H10N2S
  • Molecular Weight:178.258
Inquiry

Product Details

pd_meltingpoint:151-153 °C

Purity:99%

Quality Factory Sells Top Purity 99% 2-AMINO-4,5,6,7-TETRAHYDRO-1-BENZOTHIOPHENE-3-CARBONITRILE 4651-91-6 with Safe Delivery

  • Molecular Formula:C9H10N2S
  • Molecular Weight:178.258
  • Melting Point:151-153 °C 
  • Boiling Point:398.1 °C at 760 mmHg 
  • PKA:0.34±0.20(Predicted) 
  • Flash Point:194.6 °C 
  • PSA:78.05000 
  • Density:1.27 g/cm3 
  • LogP:2.66198 

2-AMINO-4,5,6,7-TETRAHYDRO-1-BENZOTHIOPHENE-3-CARBONITRILE(Cas 4651-91-6) Usage

InChI:InChI=1/C9H10N2S/c10-5-7-6-3-1-2-4-8(6)12-9(7)11/h1-4,11H2

4651-91-6 Relevant articles

Discovery of potent dual egfr/her2 inhibitors based on thiophene scaffold targeting h1299 lung cancer cell line

Elrayess, Ranza,Abdel Aziz, Yasmine M.,Elgawish, Mohamed Saleh,Elewa, Marwa,Yassen, Asmaa S. A.,Elhady, Sameh S.,Elshihawy, Hosam A.,Said, Mohamed M.

, p. 1 - 21 (2021)

Dual targeting of epidermal growth facto...

Synthesis, characterization, and dyeing performance of some azo thienopyridine and thienopyrimidine dyes based on wool and nylon

Regal, Mohsen K. A.,Rafat, El-Hady,El-Sattar, Nour E. A. Abd

, p. 1173 - 1182 (2020)

A string of novel heterocyclic mono azo ...

Synthesis and cytotoxicity of novel thiophene, pyran and pyridine derivatives

Wardakhan, Wagnat W.,Samir, Eman M.,El-Arab, Elham E.

, p. 259 - 270 (2018)

The reaction of 2-amino-3-cyano-tetrahyd...

Pharmacophore modeling, 3D-QSAR, synthesis, and anti-lung cancer evaluation of novel thieno[2,3-d][1,2,3]triazines targeting EGFR

Abdel Aziz, Yasmine M.,Elewa, Marwa,Elgawish, Mohamed S.,Elrayess, Ranza,Elshihawy, Hosam A.,Said, Mohamed M.

, (2020)

Two series of thieno[2,3-d][1,2,3]triazi...

Synthesis of novel 5-aryl/hetarylidenyl 3-(2-methyl-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-4-yl)-2-thioxothiazolidin-4-ones

Mendoza, Kimberly,Kamila, Sukanta,Biehl, Edward R.

, p. 741 - 753 (2014)

The synthesis of a variety of novel 5-su...

Green synthesis of biologically important 2-aminothiophenes by the mediation of ZnO@SiO2–NH2 nanoparticle as an important anti-liver cancer alternative for valproate

Gao, Feng,Yang, Jihong,Geng, Yan,Liu, Bo,Zhang, Rui,Zhang, Meng

, p. 2647 - 2654 (2021/01/29)

Liver cancer is one of the most importan...

Design, synthesis and biological evaluation of novel (E)-2-benzylidene-N-(3-cyano-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)hydrazine-1-carboxamide derivatives as α-glucosidase inhibitors

Fang, Lei,Jiang, Cheng-Shi,Li, Yue,Song, Zhiling,Wang, Kai-Ming,Xie, Hong-Xu,Zhang, Jin-He,Zhang, Juan,Zhu, Kong-Kai

supporting information, (2021/10/20)

In this present study, a series of novel...

Discovery of novel tetrahydrobenzo[b]thiophene-3-carbonitriles as histone deacetylase inhibitors

Gediya, Piyush,Vyas, Vivek K.,Carafa, Vincenzo,Sitwala, Nikum,Della Torre, Laura,Poziello, Angelita,Kurohara, Takashi,Suzuki, Takayoshi,Sanna, Vinod,Raguraman, Varalakshmi,Suthindhiran,Ghosh, Debarpan,Bhatia, Dhiraj,Altucci, Lucia,Ghate, Manjunath D.

, (2021/03/26)

The discovery and development of isoform...

4651-91-6 Process route

cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

malononitrile
109-77-3

malononitrile

3-cyano-2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene
4651-91-6

3-cyano-2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene

Conditions
Conditions Yield
With octasulfur; bovine serum albumin; In N,N-dimethyl-formamide; at 50 ℃; for 4h; Reagent/catalyst; Solvent; Time; Temperature; Concentration; Catalytic behavior;
99%
With sulfur; L-proline; In N,N-dimethyl-formamide; at 60 ℃; for 10h;
97%
With morpholine; sulfur; In ethanol; at 30 ℃; for 8h;
97%
With sulfur; diethylamine; In water; for 0.0833333h; Sonication;
96%
With sulfur; In neat (no solvent); at 100 ℃; for 4h;
96%
With sulfur; at 100 ℃; for 0.0833333h; Reagent/catalyst; Catalytic behavior; Green chemistry;
95%
With potassium carbonate; sulfur; In ethanol; at 85 ℃; for 0.25h; under 10343.2 Torr; Microwave irradiation;
95%
With sulfur; diethylamine; In ethanol; at 70 ℃; for 17h;
94%
With sulfur; potassium carbonate; In ethanol; for 3h; Reflux;
94%
With piperidine; sulfur; In methanol; at 30 ℃; for 1h;
94.9%
With sulfur; potassium fluoride on basic alumina; In ethanol; at 100 ℃; for 0.1h; under 12928.7 Torr; microwave irradiation;
92%
With sulfur; In ethanol; at 50 ℃; for 1h;
92%
With morpholine; sulfur; In ethanol; Reflux;
92%
With sulfur; calcined Mg-Al hydrotalcite; In ethanol; at 60 ℃; for 8h;
91%
With sulfur; In ethanol; at 78 ℃; for 1.08333h;
90%
With sulfur; at 100 ℃; for 2h; Reagent/catalyst; Green chemistry;
90%
With caesium carbonate; sulfur; In ethanol; for 2.33333h; Reflux;
89%
With sulfur; In ethanol; for 4h; Reflux;
89%
With sulfur; triethylamine; In water; at 20 ℃; for 6h;
89%
With morpholine; sulfur; In ethanol; at 50 - 75 ℃; for 10h;
89%
With sulfur; diethylamine; In neat (no solvent); for 0.333333h; Reagent/catalyst; Time; Milling;
88%
With sulfur; at 60 ℃; for 2h; Ionic liquid; Green chemistry;
88%
With sulfur; choline chloride; urea; sodium hydroxide; In water; at 60 ℃; Green chemistry;
88%
With sulfur; In neat (no solvent); at 60 ℃; for 2h; Reagent/catalyst; Time; Catalytic behavior;
88%
With sulfur; diethylamine; In ethanol; at 40 - 50 ℃; for 2h;
84%
cyclohexanone; malononitrile; In water; for 0.333333h; Sonication; Green chemistry;
With Na2S6; In water; for 0.5h; Reagent/catalyst; Solvent; Sonication; Green chemistry;
84%
With zinc(II) oxide; sulfur; In neat (no solvent); at 100 ℃; for 6h; Concentration; Time;
81%
With zinc ferrite; sulfur; In neat (no solvent); at 100 ℃; for 4h; Catalytic behavior; Green chemistry;
80%
With morpholine; sulfur; In ethanol; at 45 - 60 ℃; for 18.25h;
80%
With sodium aluminate; sulfur; In ethanol; at 60 ℃; for 7h;
80%
cyclohexanone; malononitrile; With diethylamine; In ethanol; for 0.166667h; Reflux;
With sulfur; In ethanol; for 3h; Reflux;
75%
cyclohexanone; malononitrile; With sulfur; In ethanol; at 20 ℃; for 0.166667h;
With morpholine; at 60 ℃; for 12h;
62.8%
With morpholine; sulfur; In ethanol; for 2h; Reflux;
57%
cyclohexanone; malononitrile; With sulfur; In ethanol; for 0.0833333h;
With morpholine; In ethanol; at 20 - 60 ℃; for 5.5h;
56%
With morpholine; cyanoacetic acid tert-butyl ester; sulfur; In ethanol; at 40 ℃; for 20h;
51%
With sulfur; triethylamine; In ethanol; for 16h; Reflux;
44%
With sulfur; triethylamine; In ethanol; for 16h; Reflux;
44%
With N-ethylmorpholine;; sulfur; In ethanol; at 20 ℃; for 3h;
33%
With sulfur; diethylamine; In ethanol;
With sulfur; diethylamine; In ethanol; at 20 ℃;
With morpholine; sulfur; In ethanol; at 0 - 20 ℃;
With morpholine; sulfur; In ethanol; for 2h; Heating;
With sulfur; triethylamine; In ethanol; for 6h; Heating / reflux;
With sulfur; diethylamine; In ethanol;
With morpholine; sulfur; In ethanol; Reflux;
With sulfur;
With sulfur; diethylamine; In ethanol; at 20 - 70 ℃;
With sulfur; triethylamine;
With morpholine; sulfur; In ethanol; Reflux;
With morpholine; sulfur;
With sulfur; diethylamine;
With morpholine; sulfur; at 20 ℃;
With morpholine; sulfur; In ethanol; at 20 ℃;
With morpholine; sulfur; In ethanol; at 60 ℃; for 12h;
With morpholine; sulfur; In ethanol; at 20 ℃;
With morpholine; sulfur; In ethanol; at 5 - 10 ℃; for 3h;
With sulfur; sodium hydroxide; In tert-butyl alcohol; at 20 ℃; for 0.5h; Reagent/catalyst; Solvent; Inert atmosphere;
94 %Chromat.
With ethanol; sulfur; triethylamine; for 0.5h; Reflux;
With sulfur; triethylamine; In ethanol; Reflux;
With morpholine; sulfur; In ethanol; at 5 - 10 ℃; for 3h;
With hydrogen sulfide; diethylamine;
With sulfur; triethylamine; In ethanol;
With morpholine; sulfur; In butan-1-ol; at 150 ℃; for 0.166667h; Cooling with ice; Microwave irradiation;
With morpholine; sulfur; In butan-1-ol; at 150 ℃; for 0.166667h; Microwave irradiation;
With morpholine; sulfur; In ethanol;
With morpholine; sulfur; In ethanol; at 60 ℃; for 24h;
With sulfur; diethylamine; In methanol;
With morpholine; sulfur; In ethanol;
With piperidine; sulfur; In ethanol; at 50 ℃; for 2h;
With sulfur; In ethanol; for 4h; Reflux;
With sulfur; In ethanol;
With morpholine; sulfur; In ethanol; at 5 - 20 ℃; for 1h;
With sulfur; In ethanol; at 60 ℃; for 1.5h;
With sulfur; In ethanol; at 60 ℃;
2-(cyclohexylidene)malononitrile
4354-73-8

2-(cyclohexylidene)malononitrile

3-cyano-2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene
4651-91-6

3-cyano-2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene

Conditions
Conditions Yield
With sulfur; tetraethylammonium hexafluorophosphate; acetonitrile; at 20 ℃; Electrolysis; Inert atmosphere;
99%
With sulfur; L-proline; In dimethyl sulfoxide; at 75 ℃;
74%
With sulfur; ethylenediamine diacetic acid;
With morpholine; sulfur; In N,N-dimethyl-formamide; at 20 - 120 ℃; for 0.166667h;
With 1,4-diaza-bicyclo[2.2.2]octane; sulfur; In water; at 20 ℃; for 7h;

4651-91-6 Upstream products

  • 108-94-1
    108-94-1

    cyclohexanone

  • 109-77-3
    109-77-3

    malononitrile

  • 4354-73-8
    4354-73-8

    2-(cyclohexylidene)malononitrile

  • 1254693-14-5
    1254693-14-5

    2-azido-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carbonitrile

4651-91-6 Downstream products

  • 23922-04-5
    23922-04-5

    2-methyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidine-4-thione

  • 4994-88-1
    4994-88-1

    5,6,7,8-tetrahydrobenzo[b]thiopheno[2,3-d]pyrimidin-4-ylamine

  • 128277-24-7
    128277-24-7

    4-chloro-2-(pyridin-3-yl)-5,6,7,8-tetrahydro-[1]-benzothieno[2,3-d]pyrimidine

  • 128277-25-8
    128277-25-8

    2-(pyridin-3-yl)-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-4-amine

Relevant Products