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15452-52-5

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15452-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15452-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15452-52:
(7*1)+(6*5)+(5*4)+(4*5)+(3*2)+(2*5)+(1*2)=95
95 % 10 = 5
So 15452-52-5 is a valid CAS Registry Number.

15452-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methanesulfonyl-4-(2-nitro-propenyl)-benzene

1.2 Other means of identification

Product number -
Other names 2-Nitro-1-(4-methylsulfon-phenyl)-propen-(1)

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:15452-52-5 SDS

15452-52-5Relevant articles and documents

Development of isoform selective PI3-kinase inhibitors as pharmacological tools for elucidating the PI3K pathway

Bruce, Ian,Akhlaq, Mohammed,Bloomfield, Graham C.,Budd, Emma,Cox, Brian,Cuenoud, Bernard,Finan, Peter,Gedeck, Peter,Hatto, Julia,Hayler, Judy F.,Head, Denise,Keller, Thomas,Kirman, Louise,Leblanc, Catherine,Grand, Darren Le,McCarthy, Clive,O'Connor, Desmond,Owen, Charles,Oza, Mrinalini S.,Pilgrim, Gaynor,Press, Nicola E.,Sviridenko, Lilya,Whitehead, Lewis

, p. 5445 - 5450 (2012/09/22)

Using a parallel synthesis approach to target a non-conserved region of the PI3K catalytic domain a pan-PI3K inhibitor 1 was elaborated to provide alpha, delta and gamma isoform selective Class I PI3K inhibitors 21, 24, 26 and 27. The compounds had good cellular activity and were selective against protein kinases and other members of the PI3K superfamily including mTOR and DNA-PK.

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