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Methyl 3-(8,13-diethyl-3,7,12,17-tetramethylporphyrin-2-yl)propanoate is a complex organic compound with the molecular formula C31H37N4O3. It is a derivative of porphyrin, a large heterocyclic aromatic organic compound consisting of four pyrrole subunits interconnected at their α-carbon atoms via methine bridges. This specific compound features two ethyl groups at the 8 and 13 positions, and four methyl groups at the 3, 7, 12, and 17 positions. The propanoate group is attached to the 2 position of the porphyrin ring, and a methyl group is present at the 3 position of the propanoate chain. methyl 3-(8,13-diethyl-3,7,12,17-tetramethylporphyrin-2-yl)propanoate is of interest in the field of chemistry, particularly in the study of porphyrins and their potential applications in areas such as medicine, materials science, and catalysis.

5174-83-4

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5174-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5174-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5174-83:
(6*5)+(5*1)+(4*7)+(3*4)+(2*8)+(1*3)=94
94 % 10 = 4
So 5174-83-4 is a valid CAS Registry Number.

5174-83-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(8,13-diethyl-3,7,12,17-tetramethyl-23,24-dihydroporphyrin-2-yl)propanoate

1.2 Other means of identification

Product number -
Other names 8,13-Diethyl-3,7,12,17-tetramethyl-21H,23H-porphine-2-propanoic acid methyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5174-83-4 SDS

5174-83-4Downstream Products

5174-83-4Relevant academic research and scientific papers

Peripheral Mercuration of Metalloporphyrins: Novel Syntheses of Deoxophylloerythroetioporphyrin and Deoxophylloerythrin Methyl Ester

Smith, Kevin M.,Langry, Kevin C.,Minnetian, Ohannes M.

, p. 4602 - 4609 (2007/10/02)

Zinc(II) porphyrins bearing unsubstituted β positions can be mercurated at the β position and at an adjacent meso position.Palladium / olefin reactions with the dimercurated porphyrins produce products possessing a five-membered isocyclic ring bridging the β and meso positions and resembling that found in chlorophyll derivatives.With use of this methodology, novel syntheses of deoxophylloerythroetioporphyrin (2) and deoxophylloerythrin methyl ester (3), two degradation products of chlorophyll, are described.

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