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130016-69-2

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130016-69-2 Usage

Methyl ester derivative

The compound is derived from alpha-methyl-1H-pyrrole-1-acetic acid by replacing the carboxylic acid group (-COOH) with a methyl ester group (-COOCH3).

Substituted pyrrole derivative

The compound is a derivative of pyrrole, which is a five-membered heterocyclic aromatic compound containing one nitrogen atom, with an additional alpha-methyl group (-CH3) attached to the ring.

Physical appearance

Colorless liquid The compound appears as a colorless liquid, which means it does not have any color when observed in its pure form.

Odor

Faint, specific odor The compound has a weak, distinct smell that can be detected at low concentrations.

Uses

Organic synthesis, pharmaceuticals, and agrochemicals 1H-Pyrrole-1-acetic acid, alpha-methyl-, methyl ester (9CI) is used as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

Chemical properties and reactivity

The compound exhibits specific chemical properties and reactivity, making it an important compound in the field of organic chemistry. This includes its ability to undergo various chemical reactions, such as esterification, amidation, and other transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 130016-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,0,1 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130016-69:
(8*1)+(7*3)+(6*0)+(5*0)+(4*1)+(3*6)+(2*6)+(1*9)=72
72 % 10 = 2
So 130016-69-2 is a valid CAS Registry Number.

130016-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-pyrrol-1-ylpropanoate

1.2 Other means of identification

Product number -
Other names 2-pyrrol-1-ylpropionic acid methyl 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:130016-69-2 SDS

130016-69-2Downstream Products

130016-69-2Relevant articles and documents

Novel Inhibitors of Hepatitis C Virus Replication

-

Page/Page column 60-61, (2009/10/21)

The embodiments provide compounds of the general Formula I, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.

THE ALKYLATION OF METHYL 2-(1-PYRROLYL)ACETATE. A NEW SYNTHETIC METHOD OF α-AMINO ACIDS

Kashima, Choji,Maruyama, Tatsuya

, p. 1727 - 1730 (2007/10/02)

The alkylation of 2-(1-pyrrolyl)acetates was accomplished by the treatment with alkyl halides in the presence of LDA to give 2-(1-pyrrolyl)alkanoates, which were convertible into α-amino acids by ozonolysis.

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