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146943-27-3

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146943-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146943-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,4 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 146943-27:
(8*1)+(7*4)+(6*6)+(5*9)+(4*4)+(3*3)+(2*2)+(1*7)=153
153 % 10 = 3
So 146943-27-3 is a valid CAS Registry Number.

146943-27-3SDS

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 methyl 3-[4-(tert-butoxycarbonyl)phenyl]propenoate

1.2 Other means of identification

Product number -
Other names 4-(tert-Butyloxycarbonyl)trans-cinnamic acid methyl ester

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:146943-27-3 SDS

146943-27-3Relevant articles and documents

Pyrrolo[2,3-d]pyrimidine thymidylate synthase inhibitors: Design and synthesis of one-carbon bridge derivatives

Aso,Imai,Yukishige,Ootsu,Akimoto

, p. 1280 - 1287 (2007/10/03)

A series of novel pyrrolo[2,3-d]pyrimidine derivatives was designed and synthesized as thymidylate synthase (TS) inhibitors. Molecular design was performed on the human TS complex model built on the basis of the reported structure of TS-deoxyuridinemonoph

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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