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119448-87-2

119448-87-2

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119448-87-2 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 28, p. 1715, 1991 DOI: 10.1002/jhet.5570280712

Check Digit Verification of cas no

The CAS Registry Mumber 119448-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,4 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119448-87:
(8*1)+(7*1)+(6*9)+(5*4)+(4*4)+(3*8)+(2*8)+(1*7)=152
152 % 10 = 2
So 119448-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O2/c1-2-14-10(13)9-8-5-3-4-6-12(8)7-11-9/h3-7H,2H2,1H3

119448-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl imidazo[1,5-a]pyridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-ethoxycarbonylimidazo<1,5-a>pyridine

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:119448-87-2 SDS

119448-87-2Relevant articles and documents

Divergent and Regioselective Synthesis of Pyrazolo[1,5- a]pyridines and Imidazo[1,5- a]pyridines

Mennie, Katrina M.,Reutershan, Michael H.,White, Catherine,Adams, Bruce,Becker, Bridget,Deng, James,Katz, Jason D.,Lablue, Elisabeth,Margrey, Kaila,Saurí, Josep

supporting information, p. 4694 - 4698 (2021/06/28)

Nitrogenous heterocycles are ubiquitous in pharmaceuticals and drug-like compounds; however, regioselective synthesis has proved challenging. Herein we report our efforts to develop a regioselective method for the synthesis of pyrazolo[1,5-a]pyridines and the serendipitous discovery of a protocol for the regioselective formation of imidazo[1,5-a]pyridines. Together, these transformations allow for the rapid and selective formation of two important heterocyclic motifs from a common intermediate.

Heterocycles from amino acids. A novel synthetic approach for imidazo[1,5-a]pyridines and imidazo[1,5-a]quinolines

Kolar,Petric,Tisler

, p. 1715 - 1720 (2007/10/02)

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