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3-[(1-acetyl-2,3-dihydro-1H-indol-5-yl)sulfonyl]propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

841275-85-2

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841275-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 841275-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,1,2,7 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 841275-85:
(8*8)+(7*4)+(6*1)+(5*2)+(4*7)+(3*5)+(2*8)+(1*5)=172
172 % 10 = 2
So 841275-85-2 is a valid CAS Registry Number.

841275-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(1-Acetyl-2,3-dihydro-1H-indol-5-yl)sulfonyl]-propanoic acid

1.2 Other means of identification

Product number -
Other names 3-[(1-acetyl-2,3-dihydro-1H-indol-5-yl)sulfonyl]propanoic 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:841275-85-2 SDS

841275-85-2Downstream Products

841275-85-2Relevant academic research and scientific papers

A convenient synthesis of novel 3-(heterocyclylsulfonyl)propanoic acids and their amide derivatives

Dorogov, Mikhail V.,Filimonov, Sergey I.,Kobylinsky, Dmitry B.,Ivanovsky, Sergey A.,Korikov, Pavel V.,Soloviev, Mikhail Y.,Khahina, Maria Y.,Shalygina, Elena E.,Kravchenko, Dmitry V.,Ivachtchenko, Alexandre V.

, p. 2999 - 3004 (2007/10/03)

A large number of novel 3-(heterocyclylsulfonyl)propanoic acids and their amide derivatives were prepared in good yields and excellent purity starting from the corresponding heterocyclic compounds. At first, chlorosulfonates were generated by reaction of initial heterocycles with various sulfonating and chlorinating agents followed by their conversion into sodium sulfinates. Treatment of sulfinates with acrylic acid smoothly afforded a series of sulfonylpropionates, which were used as convenient reagents for the preparation of a large number of the corresponding carboxamide derivatives.

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