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38664-16-3

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38664-16-3 Usage

General Description

4-(2-carboxy-ethyl)-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester is a chemical compound with the molecular formula C12H15NO4. It is an ethyl ester derivative of 4-(2-carboxy-ethyl)-2-methyl-1H-pyrrole-3-carboxylic acid. 4-(2-CARBOXY-ETHYL)-2-METHYL-1H-PYRROLE-3-CARBOXYLIC ACID ETHYL ESTER is a pyrrole derivative and belongs to the class of carboxylic acid esters. It is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active compounds. The presence of carboxylic acid and ester functional groups in this compound makes it a versatile intermediate for the synthesis of a wide range of organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 38664-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,6 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38664-16:
(7*3)+(6*8)+(5*6)+(4*6)+(3*4)+(2*1)+(1*6)=143
143 % 10 = 3
So 38664-16-3 is a valid CAS Registry Number.

38664-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-ethoxycarbonyl-5-methyl-1H-pyrrol-3-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 3-(4-ethoxycarbonyl-5-methyl-pyrrol-3-yl)-propionic acid

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:38664-16-3 SDS

38664-16-3Downstream Products

38664-16-3Relevant articles and documents

Reaction of some diketones with 5-aminolevulinic acid in acid solution

Butler,George

, p. 7017 - 7026 (2007/10/02)

Some 2,4-diketones react with 5-aminolevulinic acid in acid solution to form pyrroles. There are two modes of cyclisation, one leading to the Knorr and the other to the Fischer-Fink product. By a consideration of the products obtained from pentane-, hexane-, 3-methylpentane-, 3-isopropylpentane-, 3,3-dimethylpentane-, 1,1,1-trifluoropentane- 1,1,1,5,5,5-hexafluoro- pentane-2,4-dione and ethyl acetoacetate some generalisations concerning the formation of Knorr and Fischer-Fink products have been made. The reactions of 5-methyl-5-aminolevulinic acid with pentane- and 3-methylpentane-2,4-dione have also been examined. The relevance of these studies to the cyclic dimerisation of 5-aminolevulinic acid is discussed briefly.

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