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24509-73-7

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24509-73-7 Usage

General Description

1H-Pyrrolo[3,2-b]pyridine, 1-acetyl- (8CI) is a chemical compound consisting of a pyrrolopyridine ring with an acetyl group attached at the 1-position. It is a heterocyclic compound that is used in the synthesis of pharmaceuticals and organic compounds. 1H-Pyrrolo[3,2-b]pyridine, 1-acetyl- (8CI) has potential applications in the development of new drugs due to its unique structure and reactivity. It is also used as a building block in organic chemistry for the creation of complex molecules. 1H-Pyrrolo[3,2-b]pyridine, 1-acetyl- (8CI) is a valuable chemical in the field of medicinal and synthetic chemistry, with potential for various applications in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 24509-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,0 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24509-73:
(7*2)+(6*4)+(5*5)+(4*0)+(3*9)+(2*7)+(1*3)=107
107 % 10 = 7
So 24509-73-7 is a valid CAS Registry Number.

24509-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Acetyl-1H-pyrrolo[3,2-b]pyridine

1.2 Other means of identification

Product number -
Other names 1-(1H-pyrrolo[3,2-b]pyridin-1-yl)ethanone

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:24509-73-7 SDS

24509-73-7Relevant articles and documents

Site-selective azaindole arylation at the azine and azole rings via N-oxide activation

Huestis, Malcolm P.,Fagnou, Keith

supporting information; experimental part, p. 1357 - 1360 (2009/09/05)

Subjection of N-methyl 6-and 7-azaindole N-oxides to a Pd(OAc) 2/DavePhos catalyst system enables regioselective direct arylation of the azine ring. Following deoxygenation, 7-azaindole substrates undergo an additional regioselective azole direct arylation event in good yield.

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