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919116-69-1

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919116-69-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 919116-69-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,1,1 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 919116-69:
(8*9)+(7*1)+(6*9)+(5*1)+(4*1)+(3*6)+(2*6)+(1*9)=181
181 % 10 = 1
So 919116-69-1 is a valid CAS Registry Number.

919116-69-1SDS

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 4-[(6-oxo-1H-pyrimidin-2-yl)amino]benzoic acid

1.2 Other means of identification

Product number -
Other names 4-(6-oxo-1,6-dihydropyrimidin-2-ylamino)benzoic acid

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:919116-69-1 SDS

919116-69-1Relevant articles and documents

New compounds

-

Page/Page column 18, (2009/07/10)

The present invention encompasses compounds of general formula (1) wherein R1, R2, R4, X, m, n and p are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, and their use for preparing a pharmaceutical composition having the above-mentioned properties.

Design and preparation of 2-benzamido-pyrimidines as inhibitors of IKK

Waelchli, Rudolf,Bollbuck, Birgit,Bruns, Christian,Buhl, Thomas,Eder, Joerg,Feifel, Roland,Hersperger, Rene,Janser, Philipp,Revesz, Laszlo,Zerwes, Hans-Guenter,Schlapbach, Achim

, p. 108 - 112 (2007/10/03)

The design, synthesis, and the biological evaluation of 2-benzamido-pyrimidines as novel IKK inhibitors are described. By optimization of the lead compound 3, compounds 16 and 24 are identified as good inhibitors of IKK2 with IC50 values of 40 and 25 nM, respectively. Compound 16 also demonstrated significant in vivo activity in an acute model of cytokine release.

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