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612097-74-2

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612097-74-2 Usage

Structure

Ethyl ester derivative of 4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-1-piperidinecarboxylic acid

Receptor interaction

Potent and selective antagonist of the adenosine A1 receptor

Therapeutic applications

Potential use in the treatment of various diseases and disorders, including cardiovascular and neurodegenerative conditions

Analgesic and anxiolytic properties

Has shown promise as an analgesic and anxiolytic agent

Research and development

Further studies may lead to the discovery of new pharmaceutical drugs with improved efficacy and safety profiles

Check Digit Verification of cas no

The CAS Registry Mumber 612097-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,0,9 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 612097-74:
(8*6)+(7*1)+(6*2)+(5*0)+(4*9)+(3*7)+(2*7)+(1*4)=142
142 % 10 = 2
So 612097-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H19N3O2/c1-2-20-15(19)18-8-5-11(6-9-18)13-10-17-14-12(13)4-3-7-16-14/h3-4,7,10-11H,2,5-6,8-9H2,1H3,(H,16,17)

612097-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-(1H-pyrrolo[2,3-b]pyridin-3-yl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Piperidinecarboxylic acid,4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-,ethyl ester

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:612097-74-2 SDS

612097-74-2Downstream Products

612097-74-2Relevant articles and documents

Synthesis and structure-activity relationships of piperidinylpyrrolopyridine derivatives as potent and selective H1 antagonists

Fonquerna, Silvia,Miralpeix, Montse,Pages, Lluis,Puig, Carles,Cardus, Arantxa,Anton, Francisca,Vilella, Dolors,Aparici, Monica,Prieto, Jose,Warrellow, Graham,Beleta, Jorge,Ryder, Hamish

, p. 1165 - 1167 (2005)

The synthesis and structure-activity relationships of piperidinylpyrrolopyridines as potent and selective H1 antagonists are discussed. It was found that the nature of the acid chain bonded to piperidine was a key feature for maintaining both the duration of action in vivo and lack of sedative properties.

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