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2-Benzothiazolepropanoicacid,methylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

610277-15-1

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610277-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 610277-15-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,0,2,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 610277-15:
(8*6)+(7*1)+(6*0)+(5*2)+(4*7)+(3*7)+(2*1)+(1*5)=121
121 % 10 = 1
So 610277-15-1 is a valid CAS Registry Number.

610277-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-(1,3-benzothiazol-2-yl)propanoate

1.2 Other means of identification

Product number -
Other names methyl 3-benzothiazol-2-ylpropanoate

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:610277-15-1 SDS

610277-15-1Relevant academic research and scientific papers

HYDROXYL PURINE COMPOUNDS AND USE THEREOF

-

Paragraph 0324; 0325, (2018/04/05)

Disclosed are a series of hydroxyl purine compounds and the use thereof as PDE2 or TNFα inhibitors, in particular, the compounds as shown in formula (I), or tautomers thereof or pharmaceutically acceptable salts thereof.

Iron-catalyzed C-H alkylation of heterocyclic C-H bonds

Babu, Kaki Raveendra,Zhu, Nengbo,Bao, Hongli

supporting information, p. 46 - 49 (2017/11/28)

An efficient, iron-catalyzed C-H alkylation of benzothiazoles by using alkyl diacyl peroxides and alkyl tertbutyl peresters which are readily accessible from carboxylic acids to synthesize 2-alkylbenzothiazoles is developed. This reaction is environmentally benign and compatible with a broad range of functional groups. Various primary, secondary, and tertiary alkyl groups can be efficiently incorporated into diverse benzothiazoles. The effectiveness of this method is illustrated by late-stage functionalization of biologically active heterocycles.

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