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118757-13-4

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118757-13-4 Usage

Molecular weight

315.37 g/mol

Physical state

White to off-white solid

Solubility

Slightly soluble in water, more soluble in organic solvents

Derivative

Ester derivative of 1H-indole-5-carboxylic acid

Use

Building block in organic synthesis, particularly in the preparation of pharmaceutical compounds

Versatility

Phenylsulfonyl group attached to the indole ring makes it a versatile intermediate for the construction of diverse molecules with potential biological activity

Reactant

Used in the production of other complex organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 118757-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,5 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118757-13:
(8*1)+(7*1)+(6*8)+(5*7)+(4*5)+(3*7)+(2*1)+(1*3)=144
144 % 10 = 4
So 118757-13-4 is a valid CAS Registry Number.

118757-13-4SDS

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 ethyl 1-(benzenesulfonyl)indole-5-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1-phenylsulfonylindole-5-carboxylate

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:118757-13-4 SDS

118757-13-4Downstream Products

118757-13-4Relevant articles and documents

Discovery and synthesis of 2-amino-1-methyl-1H-imidazol-4(5H)-ones as GPCR ligands; an approach to develop breast cancer drugs via GPCR associated PAR1 and PI3Kinase inhibition mechanism

Ashok,Shivananda,Manikandan,Chandrasekaran

, p. 641 - 651 (2019/02/26)

Efforts were taken to synthesis and characterize 2-amino-1-methyl-1H-imidazole-4(5H)-one derivatives (4a-u) through a four-step reaction. The achieved compounds in remarkable yield have characterized through standard analytical techniques such as FTIR, LC

THE MANGANESE(III) ACETATE OXIDATION OF N-PROTECTED INDOLINES

Ketcha, Daniel M.

, p. 2151 - 2154 (2007/10/02)

A variety of N-protected indolines can be oxidized to the corresponding indoles using manganese(III) acetate in glacial acetic acid.

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