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121638-36-6

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121638-36-6 Usage

General Description

Benzofuran-5-yl-acetic acid Methyl ester, also known as 5-(methoxycarbonyl)benzofuran, is a synthetic organic compound with a chemical formula C11H10O4. It is a methyl ester of benzofuran-5-yl-acetic acid, which is commonly used in pharmaceutical research as a building block for the synthesis of various bioactive compounds. Benzofuran-5-yl-acetic acid Methyl ester has potential pharmacological properties and is being investigated for its potential use in the development of new drugs for various medical conditions. The compound has also been studied for its potential role in the treatment of neurological disorders and cancer. Its chemical structure and properties make it a valuable compound for medicinal chemistry research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 121638-36-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,3 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 121638-36:
(8*1)+(7*2)+(6*1)+(5*6)+(4*3)+(3*8)+(2*3)+(1*6)=106
106 % 10 = 6
So 121638-36-6 is a valid CAS Registry Number.

121638-36-6SDS

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 methyl 2-cyclopenta[c]pyran-1-ylacetate

1.2 Other means of identification

Product number -
Other names 5-Benzofuranacetic 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:121638-36-6 SDS

121638-36-6Relevant articles and documents

Palladium/TY-Phos-Catalyzed Asymmetric Intermolecular α-Arylation of Aldehydes with Aryl Bromides

Li, Wenbo,Liu, Feng,Pan, Zhangjin,Wu, Hai-Hong,Zhang, Junliang,Zhu, Shuai

supporting information, p. 18542 - 18546 (2021/07/21)

Despite much progress has been made in the asymmetric α-arylation reactions of cyclic ketones, lactones and lactams, the enantioselective α-arylation of acyclic carbonyl compounds lagged much behind due to the in situ generated Z/E-enolate intermediates l

Assay for evaluating inhibition of polymorphonuclear leukocyte elastase by N-substituted azetidinones

-

, (2008/06/13)

-

PREPARATION AND CYCLIZATION OF ARYLOXYACETALDEHYDE ACETALS; A GENERAL SYNTHESIS OF 2,3-UNSUBSTITUTED BENZOFURANS

Barker, Peter,Finke, Paul,Thompson, Kevan

, p. 257 - 266 (2007/10/02)

A improved method for the preparation of 2,3-unsubstituted benzofurans is described.Specifically, the PPA catalysed cyclization of aryloxyacetaldehyde acetals to give (4-7)-substituted benzofurans has been achieved.

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