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129090-35-3

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129090-35-3 Usage

Chemical structure

Pyridine ring with an amino group at 2-position, cyano group at 3-position, methyl group at 6-position, and pyridyl group at 5-position

Use

Building block in synthesis of pharmaceuticals and agrochemicals

Potential biological activity

Valuable target for medicinal chemistry research

Applications

Materials science and industrial processes due to varied chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 129090-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,9 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 129090-35:
(8*1)+(7*2)+(6*9)+(5*0)+(4*9)+(3*0)+(2*3)+(1*5)=123
123 % 10 = 3
So 129090-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N4/c1-8-11(9-2-4-15-5-3-9)6-10(7-13)12(14)16-8/h2-6H,1H3,(H2,14,16)

129090-35-3SDS

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 2-amino-6-methyl-5-pyridin-4-ylpyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 6-amino-2-methyl-3,4'-bipyridine-5-carbonitrile

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:129090-35-3 SDS

129090-35-3Downstream Products

129090-35-3Relevant articles and documents

Novel cAMP PDE III inhibitors: Imidazo[4,5-b]pyridin-2(3H)-ones and thiazolo[4,5-b]pyridin-2(3H)-ones and their analogs

Singh,Bacon,Robinson,Fritz,Lesher,Kumar,Dority,Reuman,Kuo,Eissenstat,Pagani,Bode,Bentley,Connell,Hamel,Silver

, p. 248 - 254 (2007/10/02)

The transformation of milrinone to 1,3-dihydro-5-methyl-6-(4-pyridinyl)- 2H-imidazo[4,5-b]pyridin-2-one (13a), 5-methyl-6-(4-pyridinyl)thiazolo[4,5- b]pyridin-2(3H)-one (51), and 7-methyl-6-(4-pyridinyl)-1,8-naphthyridin- 2(1H)-one (22) resulted in very p

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