Cas 168974-89-8,(1R,cis)-3-<<2-amino-6-chloro-5-(4-chlorophenylazo)pyrimidin-4-yl>aminomethyl>-1,2,2-trimethylcyclopentylmethanol

168974-89-8

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Basic information

Product Name: (1R,cis)-3-<<2-amino-6-chloro-5-(4-chlorophenylazo)pyrimidin-4-yl>aminomethyl>-1,2,2-trimethylcyclopentylmethanol
Synonyms: (1R,cis)-3-<<2-amino-6-chloro-5-(4-chlorophenylazo)pyrimidin-4-yl>aminomethyl>-1,2,2-trimethylcyclopentylmethanol
CAS NO:168974-89-8
Molecular Formula:
Molecular Weight: 437.372
EINECS: N/A
Product Categories: N/A

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: (1R,cis)-3-<<2-amino-6-chloro-5-(4-chlorophenylazo)pyrimidin-4-yl>aminomethyl>-1,2,2-trimethylcyclopentylmethanol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,cis)-3-<<2-amino-6-chloro-5-(4-chlorophenylazo)pyrimidin-4-yl>aminomethyl>-1,2,2-trimethylcyclopentylmethanol(168974-89-8)
EPA Substance Registry System: (1R,cis)-3-<<2-amino-6-chloro-5-(4-chlorophenylazo)pyrimidin-4-yl>aminomethyl>-1,2,2-trimethylcyclopentylmethanol(168974-89-8)

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: 168974-89-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 168974-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,9,7 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 168974-89:
(8*1)+(7*6)+(6*8)+(5*9)+(4*7)+(3*4)+(2*8)+(1*9)=208
208 % 10 = 8
So 168974-89-8 is a valid CAS Registry Number.

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168974-89-8Relevant academic research and scientific papers

Synthesis and antiviral and cytostatic activities of carbocyclic nucleosides incorporating a modified cyclopentane ring. 1: Guanosine analogues

Blanco,Caamano,Fernandez,Gomez,Nieto,Balzarini,Padalko,De Clercq

, p. 159 - 171 (1997)

Six new carbocyclic nucleosides were prepared by constructing a guanine (compounds 6, 8 and 10) or 8-azaguanine (compounds 7, 9 and 11) base on the amino group of (1R, cis)-3-(aminomethyl)-1,2,2-trimethylcyclopentylmethanol (2), and their activities again

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