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134372-99-9

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134372-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134372-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,3,7 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134372-99:
(8*1)+(7*3)+(6*4)+(5*3)+(4*7)+(3*2)+(2*9)+(1*9)=129
129 % 10 = 9
So 134372-99-9 is a valid CAS Registry Number.

134372-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-[2,2-dimethylethyl]carboxyphenyl)-1-propanal

1.2 Other means of identification

Product number -
Other names .3-[4-(2,2-dimethylethyl)carboxyphenyl]-1-propanal

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:134372-99-9 SDS

134372-99-9Relevant articles and documents

Novel P2X7 receptor antagonists.

Alcaraz,Baxter,Bent,Bowers,Braddock,Cladingboel,Donald,Fagura,Furber,Laurent,Lawson,Mortimore,McCormick,Roberts,Robertson

, p. 4043 - 4046 (2007/10/03)

The synthesis and pharmacological evaluation of a new series of potent P2X(7) receptor antagonists is disclosed. The compounds inhibit BzATP-mediated pore formation in THP-1 cells. The distribution of the P2X(7) receptor in inflammatory cells, most notabl

A Novel Synthetic Approach to Pyrrolopyrimidine Antifolates

Miwa, Tetsuo,Hitaka, Takenori,Akimoto, Hiroshi

, p. 1696 - 1701 (2007/10/02)

A novel and efficient synthetic method for the synthesis of pyrrolopyrimidine antifolates is described.The key reaction of this method is the photo-initiated free radical addition of bromomalononitrile or ethyl bromocyanoacetate to an enol ether to afford the backbone skeleton of the targeted antifolate molecule.The key intermediates 3 or 4 are smoothly converted to the pyrrolopyrimidine antifolates 1 or 2 in three steps and in high overall yield.

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