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908808-35-5

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908808-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 908808-35-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,8,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 908808-35:
(8*9)+(7*0)+(6*8)+(5*8)+(4*0)+(3*8)+(2*3)+(1*5)=195
195 % 10 = 5
So 908808-35-5 is a valid CAS Registry Number.

908808-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Amino-3-methyl-1H-pyrazole-4-carboxamide sulfate (1:1)

1.2 Other means of identification

Product number -
Other names 5-amino-3-methyl-1H-pyrazole-4-carboxylic acid amide

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:908808-35-5 SDS

908808-35-5Relevant articles and documents

PYRAZOLO[3,4-d]PYRIMIDINE DERIVATIVES

-

Page/Page column 6, (2009/03/07)

Disclosed are novel pyrazolo[3,4-d]pyrimidine derivatives that are inhibitors of Raf kinase. These compounds and their pharmaceutically-acceptable salts and esters are anti-proliferative agents useful in the treatment or control of proliferative disorders such as solid tumors, in particular breast tumor, colon tumor, lung tumor, prostate tumor, and melanoma. Also disclosed are a composition and a unit dose formulation comprising such a compound, or a pharmaceutically-acceptable salt or ester thereof, methods for making such compounds, and methods for using such compounds, or their pharmaceutically-acceptable salts or esters, in the treatment of proliferative disorders.

Guanosine Analogues. Synthesis of Nucleosides of Certain 3-Substituted 6-Aminopyrazolopyrimidin-4(5H)-ones as Potential Immunotherapeutic Agents

Bontems, Roger J.,Anderson, Jack D.,Smee, Donald F.,Jin, Ai,Alaghamandan, Hassan A.,et al.

, p. 2174 - 2178 (2007/10/02)

Several guanosine analogues were synthesized in the pyrazolopyrimidine ring system with various substituents at the 3-position.The new analogues prepared here include the CH3 (2-amino-3-methyl-1-β-D-ribofuranosylpyrazolopyrimidin-4(5H)-one,

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