Cas 1268853-91-3,2-(4-chlorophenyl)-5-(hydroxymethyl)-4-phenyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-b]pyridine-6,7-diol

1268853-91-3

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Basic information

Product Name: 2-(4-chlorophenyl)-5-(hydroxymethyl)-4-phenyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-b]pyridine-6,7-diol
Synonyms:
CAS NO:1268853-91-3
Molecular Formula:
Molecular Weight: 371.823
EINECS: N/A
Product Categories: N/A
Mol File: 1268853-91-3.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(4-chlorophenyl)-5-(hydroxymethyl)-4-phenyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-b]pyridine-6,7-diol(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-chlorophenyl)-5-(hydroxymethyl)-4-phenyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-b]pyridine-6,7-diol(1268853-91-3)
EPA Substance Registry System: 2-(4-chlorophenyl)-5-(hydroxymethyl)-4-phenyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-b]pyridine-6,7-diol(1268853-91-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1268853-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1268853-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,8,5 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1268853-91:
(9*1)+(8*2)+(7*6)+(6*8)+(5*8)+(4*5)+(3*3)+(2*9)+(1*1)=203
203 % 10 = 3
So 1268853-91-3 is a valid CAS Registry Number.

1268853-91-3Upstream product

1268853-91-3Downstream Products

1268853-91-3Relevant articles and documents

Carbohydrate building blocks in the Ugi three-component coupling reaction: Convenient annulation of iminosugars on imidazoles

Rai, Vijai K.,Singh, Santosh,Singh, Pankaj,Yadav, Lal Dhar S.

, p. 4051 - 4056 (2010)

An unprecedented version of the Ugi three-component coupling reaction is reported in which isocyanides react with unprotected aldoses as biorenewable aldehyde components and acyclic amidines as amine components. The reaction proceeds through [4 + 1] cyclo

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