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ETHYL N-6-PYRIDINO-IMIDAZOLE-2-METHYL-3-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87597-23-7

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87597-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87597-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,9 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87597-23:
(7*8)+(6*7)+(5*5)+(4*9)+(3*7)+(2*2)+(1*3)=187
187 % 10 = 7
So 87597-23-7 is a valid CAS Registry Number.

87597-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-methylimidazo[1,2-a]pyrazine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 2-methyl-imidazo[1,2-a]pyrazine-3-carboxylic acid 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:87597-23-7 SDS

87597-23-7Relevant academic research and scientific papers

NOVEL OXADIAZOLE COMPOUNDS

-

Page/Page column 145, (2011/06/26)

Novel oxadiazole compounds, pharmaceutical compositions containing such compounds and the use of those compounds or compositions as agonists or antagonists of the S1P family of G protein-coupled receptors for treating diseases associated with modulation o

NOVEL OXADIAZOLE COMPOUNDS

-

Page/Page column 118, (2008/12/06)

Novel oxadiazole compounds, pharmaceutical compositions containing such compounds and the use of those compounds or compositions as agonists or antagonists of the S1P family of G protein-coupled receptors for treating diseases associated with modulation o

Research on heterocyclic compounds. XVI. 2-Methylimidazo[1,2-a]pyrazine-3-carboxylic acids

Abignente,Arena,De Caprariis,et al.

, p. 79 - 85 (2007/10/02)

A group of 2-methylimidazo[1,2-a]pyrazine-3-carboxylic acids bearing various substituents on the pyrazine ring was synthesized by the reaction of a 2-aminopyrazine with ethyl 2-chloroacetoacetate; the ethyl carboxylates so obtained gave the corresponding acids by hydrolysis. The mechanism of this synthesis was discussed. Antiinflammatory and related pharmacological activities of these carboxylic acids were compared with indomethacin.

Synthesis of imidazo[1,2-a]pyrazine derivatives with uterine-relaxing, antibronchospastic, and cardiac-stimulating properties

Sablayrolles,Cros,Milhavet,Rechenq,Chapat,Boucard,Serrano,McNeill

, p. 206 - 212 (2007/10/02)

A series of imidazo[1,2-a]pyrazine derivatives was synthesized by condensation of α-halogenocarbonyl compounds and aminopyrazines. Various compounds resulted from competitive reactions or reagent isomerization and demonstrated in vitro uterine-relaxing and in vivo antibronchospastic activities. On isolated atria, 5-bromoimidazo[1,2-a]pyrazine showed positive chronotropic and inotropic properties; the latter was associated with an increase in the cyclic AMP tissue concentration. Potentiation of the isoproterenol positive inotropic effect of 5-bromoimidazo[1,2-a]pyrazine and the lack of blockade of the 5-bromoimidazo[1,2-a]pyrazine positive inotropic effect by propranolol suggested phosphodiesterase-inhibiting properties.

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