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245064-80-6

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245064-80-6 Usage

Chemical Class

Pyrrolopyridine derivatives

Contains

Carboxylic acid and phenylsulfonyl group

Potential Applications

Medicinal chemistry, drug discovery, antimicrobial, antiviral, and anticancer properties

Use as Building Block

Synthesis of various organic compounds

Versatility

Valuable for research and development in pharmaceuticals and organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 245064-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,0,6 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 245064-80:
(8*2)+(7*4)+(6*5)+(5*0)+(4*6)+(3*4)+(2*8)+(1*0)=126
126 % 10 = 6
So 245064-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O4S/c17-14(18)12-9-16(13-11(12)7-4-8-15-13)21(19,20)10-5-2-1-3-6-10/h1-9H,(H,17,18)

245064-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfonyl)pyrrolo[2,3-b]pyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-Phenylsulfonylpyrrolo[2,3-b]pyridine-3-carboxylic 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:245064-80-6 SDS

245064-80-6Relevant articles and documents

Synthesis of indolo[3,2-c]quinoline and pyrido[3',2':4,5][3,2- c]quinoline derivatives

Mouaddib, Abderrahim,Joseph, Beno?t,Hasnaoui, Aissa,Mérour, Jean-Yves

, p. 549 - 556 (2007/10/03)

Potential antitumoral scaffold indolo[3,2-c]quinoline 5a was obtained by an intramolecular Heck cyclisation from the corresponding 2-iodophenyl-3- indolecarboxamide 4a. The 7-azaindole analogue 5b was prepared by the same approach. Triflate displacement o

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