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1H-Imidazo[4,5-b]pyridine-6-carbonitrile, 5-amino- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50738-98-2

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50738-98-2 Usage

Heterocyclic compound

Imidazole and pyridine rings The compound consists of two heterocyclic rings, which are imidazole and pyridine, containing different combinations of carbon and nitrogen atoms.

Carbonitrile group

Cyano functional group (-CN) A cyano group, which is a carbon atom triple-bonded to a nitrogen atom, is present in the compound.

Amino group

5-aminodesignation An amino group (-NH2) is attached to the 5th carbon atom of the imidazo[4,5-b]pyridine ring, giving the compound its 5-aminodesignation.

Biological activity

Potential pharmaceutical or biological applications The compound may have potential applications in pharmaceuticals or biology due to its unique structure, which combines features of two important classes of biologically active molecules.

Further research needed

Specific properties and applications The properties and potential applications of 1H-Imidazo[4,5-b]pyridine-6-carbonitrile, 5-amino- (9CI) would need to be investigated through research and experimentation to fully understand its potential.

Check Digit Verification of cas no

The CAS Registry Mumber 50738-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,3 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50738-98:
(7*5)+(6*0)+(5*7)+(4*3)+(3*8)+(2*9)+(1*8)=132
132 % 10 = 2
So 50738-98-2 is a valid CAS Registry Number.

50738-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-1H-imidazo[4,5-b]pyridine-6-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-Aminoimid<pyrido-6-carbonitril

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:50738-98-2 SDS

50738-98-2Relevant academic research and scientific papers

Syntheses of 8-aminoimidazor[4′,5′:5,6]pyrido[2,3-d]pyrimidines: Linear tricyclic analogs of adenine

Harris, Philip A.,Pendergast, William

, p. 319 - 322 (1996)

The syntheses of 8-aminoimidazo[4′,5′:5,6]pyrido[2,3-d]pyrimidines (7), stretched-out versions of the naturally occuring nucleoside base adenine, are reported. Their preparation involves conversion of purine into 5-aminoimidazo[4,5-b]pyrimidine-6-carbonitrile (1) by reaction with malononitrile, followed by construction of the pyrimidine ring in two steps via the ethoxymethylene derivative 3. 8-Azapurine can be converted to 8-amino-1,2,3-triazolo[4′,5′:5,6]pyrido[2,3-d]pyrimidines 8 in a similar fashion.

RNA-SELECTIVE HYBRIDIZATION REAGENT AND UTILIZATION OF THE SAME

-

Page/Page column 14-15, (2011/01/12)

Provided is a nucleoside derivative which has a high affinity for RNA. Use is made of a nucleoside derivative represented by either formula (1) or formula (2). (In formulae (1) and (2), Z represents a carbon atom or a nitrogen atom; R1 represen

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