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1H-Pyrrole-3,4-dipropanoic acid, 2-methyl-5-[(phenylmethoxy)carbonyl]-, dimethyl ester is a complex organic compound with the molecular formula C18H21NO4. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with one nitrogen atom and four carbon atoms. In this specific compound, the pyrrole ring is substituted with two propanoic acid groups at positions 3 and 4, a methyl group at position 2, and a phenylmethoxycarbonyl group at position 5. The dimethyl ester functional group indicates that the two carboxylic acid groups are esterified with methanol, resulting in a more stable and less reactive compound. This chemical is primarily used in the synthesis of various pharmaceuticals and biologically active molecules due to its unique structure and properties.

73870-06-1

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73870-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73870-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,7 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73870-06:
(7*7)+(6*3)+(5*8)+(4*7)+(3*0)+(2*0)+(1*6)=141
141 % 10 = 1
So 73870-06-1 is a valid CAS Registry Number.

73870-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl-5-benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-2-methylpyrrol-3-propionat

1.2 Other means of identification

Product number -
Other names 3,4-Bis-(2-methoxycarbonyl-ethyl)-5-methyl-1H-pyrrole-2-carboxylic acid benzyl ester

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:73870-06-1 SDS

73870-06-1Relevant academic research and scientific papers

Tetrapyrrole Biosynthesis, 9. - Synthesis of Protected Nor- and Homoporphobilinogen

Franck, Burchhard,Wegner, Christian,Bringmann, Gerhard,Fels, Gregor

, p. 253 - 262 (2007/10/02)

The monopyrroles norporphobilinogen (3) and homoporphobilinogen (4) , being derivates of the biogenetic porphyrin precursor porphobilinogen (1), are of topical interest for biomimetic porphyrin syntheses.Syntheses were developed for the protected " depot

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