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10589-94-3

  • Product Name:Pyroporphyrin dimethyl ester
  • Molecular Formula:C32H34N4O4
  • Molecular Weight:538.646
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Product Details

pd_meltingpoint:217-220 °C(lit.)

Purity:99%

High Quality Chinese Manufacturer supply 10589-94-3 Pyroporphyrin dimethyl ester

  • Molecular Formula:C32H34N4O4
  • Molecular Weight:538.646
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:217-220 °C(lit.) 
  • Refractive Index:1.602 
  • Boiling Point:996.386 °C at 760 mmHg 
  • Flash Point:556.394 °C 
  • PSA：108.90000 
  • Density:1.227 g/cm3 
  • LogP:3.01820 

Pyroporphyrin dimethyl ester(Cas 10589-94-3) Usage

InChI:InChI=1/C32H34N4O4/c1-17-11-22-14-27-19(3)23(7-9-31(37)39-5)29(35-27)16-30-24(8-10-32(38)40-6)20(4)28(36-30)15-26-18(2)12-21(34-26)13-25(17)33-22/h11-16,34-35H,7-10H2,1-6H3/b21-13-,22-14-,25-13-,26-15-,27-14-,28-15-,29-16-,30-16-

10589-94-3 Relevant articles

Synthesis and structure of five or six-coordinate manganese deuteroporphyrin-niacin dyads with intramolecular axial pyridine

Sun, Chengguo,Hu, Bingcheng,Zhao, Donghui,Liu, Zuliang

, p. 130 - 137,8 (2013)

Deuteroporphyrin-niacin dyads with diffe...

-

Snellgrove,Plane

, p. 3185 (1968)

-

Simple and efficient method for synthesis of metallodeutero-porphyrin derivatives bearing symmetrical disulphide bond

Sun, Cheng Guo,Hu, Bing Cheng,Zhou, Wei You,Xu, Shi Chao,Deng, Quan Zhi,Liu, Zu Liang

, p. 527 - 530 (2011)

A novel thiol-derivative porphyrin [2,7,...

A facile synthesis of deuteroporphyrins derivatives under ultrasound irradiation

Hu, Bingcheng,Zhou, Weiyou,Tang, Ying,Huang, Chengmei,Liu, Zuliang

, p. 288 - 291 (2010)

A facile, efficient and general method f...

PETROPORPHYRINS - II. THE PRESENCE OF PORPHYRINS WITH EXTENDED ALKYL SUBSTITUENTS

Martin, J.,Quirke, E.,Shaw, George J.,Soper, Paul D.,Maxwell, James R.

, p. 3261 - 3268 (1980)

The vanadyl porphyrins from Boscan oil (...

Dynamic docking and electron transfer between Zn-myoglobin and cytochrome b5

Liang, Zhao-Xun,Nocek, Judith M.,Huang, Kai,Hayes, Ryan T.,Kurnikov, Igor V.,Beratan, David N.,Hoffman, Brian M.

, p. 6849 - 6859 (2002)

We present a broad study of the effect o...

Synthesis of tetrapyrrole nitrogen mustards with potential anti-tumor activities

Chen, Zhi-Long,Wan, Wei-Qin,Chen, Jing-Rong,Zhao, Fang,Xu, De-Yu

, p. 1739 - 1745 (1998)

Eight porphyrin nitrogen mustards and si...

Benzoylation at the meso position of a zinc(II) deuteroporphyrin

Vazquez, Jordi,Gonzalez, Maria M.,Marti, Cristina,Nonell, Santi,Trull, Francesc R.

, p. 69 - 79 (1998)

By short treatment of zinc(II) deuteropo...

Formyl-and acetyl-substituted deuteroporphyrines

Brockmann Jr.,Bliesener,Inhoffen

, p. 148 - 161 (1968)

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On further knowledge of chlorophyll and hemin. VII. On meso-oxo-porphinogens

Inhoffen,Fuhrhop,von der Haar

, p. 92 - 105 (1966)

-

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Miller,Rapoport

, p. 3479 (1977)

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Protonation-deprotonation equilibria in tetrapyrroles Part 4: Mono- and diprotonations of deutero-, hemato-, meso-, and protoporphyrin IX dimethyl esters in methanolic hydrochloric acid

Hynninen, Paavo H.

, p. 385 - 395 (2015/05/20)

The N-protonations in the deutero, hemat...

Synthesis and catalytic properties of a series of cobalt porphyrins as cytochrome P450 model: The effect of substituents on the catalytic activity

Hu, Bingcheng,Sun, Chengguo,Deng, Quanzhi,Liu, Zuliang

, p. 345 - 352 (2013/07/26)

A series of cobalt porphyrins derived fr...

Rapid aerobic oxidation of alcohols to carbonyl compounds with dioxygen using metallodeuteroporphyrin dimethyl esters as catalysts in the presence of isobutylaldehyde

Sun, Chengguo,Hu, Bingcheng,Liu, Zuliang

experimental part, p. 295 - 303 (2012/07/28)

A facile biomimetic method for rapid oxi...

10589-94-3 Process route

methanol
67-56-1

methanol

deuterohemin chloride
21007-21-6

deuterohemin chloride

deuteroporphyrin IX dimethyl ester
81971-99-5,10589-94-3

deuteroporphyrin IX dimethyl ester

Conditions
Conditions Yield
With sulfuric acid; at 20 ℃; Sonication;
97%
methanol
67-56-1

methanol

deuteroporphyrin IX

deuteroporphyrin IX

deuteroporphyrin IX dimethyl ester
81971-99-5,10589-94-3

deuteroporphyrin IX dimethyl ester

Conditions
Conditions Yield
With sulfuric acid; for 18h; Ambient temperature;
93.4%
With hydrogenchloride;
With hydrogenchloride;
With sulfuric acid; for 1h; Irradiation;

10589-94-3 Upstream products

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    186581-53-3

    diazomethane

  • 67-56-1
    67-56-1

    methanol

  • 56674-10-3
    56674-10-3

    diethyl 2,7,12,18-tetramethyl-13,17-bis<β-(methoxycarbonyl)ethyl>porphyrin-3,8-dicarboxylate

  • 21007-21-6
    21007-21-6

    deuterohemin chloride

10589-94-3 Downstream products

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    5522-66-7

    3,3'-(3,7,12,17-tetramethyl-8,13-divinyl-21H,23H-porphine-2,18-diyl)-bis-propionic acid dimethyl ester

  • 10591-31-8
    10591-31-8

    2,4-diacetyl-6,7-bis<2-(methoxycarbonyl)ethyl>-1,3,5,8-tetramethylporphyrin

  • 15295-27-9
    15295-27-9

    3,3'-<3-Acetyl-2,7,12,18-tetramethyl-21H,23H-porphyrin-13,17-diyl>dipropionsaeure-dimethylester

  • 15295-25-7
    15295-25-7

    3,3'-<8-Acetyl-2,7,12,18-tetramethyl-21H,23H-porphyrin-13,17-diyl>dipropionsaeure-dimethylester

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