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149325-57-5

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149325-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149325-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,3,2 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 149325-57:
(8*1)+(7*4)+(6*9)+(5*3)+(4*2)+(3*5)+(2*5)+(1*7)=145
145 % 10 = 5
So 149325-57-5 is a valid CAS Registry Number.

149325-57-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(3-hydroxy-1-methylpropyl)benzoate

1.2 Other means of identification

Product number -
Other names t-Butyl 4-(3-hydroxy-1-methylpropyl) benzoate

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:149325-57-5 SDS

149325-57-5Relevant 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

Novel 6-5 fused ring heterocycle antifolates with potent antitumor activity: Bridge modifications and heterocyclic benzoyl isosters of 2,4-diamino-6,7-dihydro-5H-cyclopenta[d]pyrimidine antifolate

Kotake,Okauchi,Iijima,Yoshimatsu,Nomura

, p. 829 - 841 (2007/10/02)

Structural modifications of an extremely potent inhibitor of dihydrofolate reductase (DHFR) activity and tumor cell growth, N-[4-[3-(2,4-diamino-6,7-dihydro-5H-cyclopenta[d]pyrimidin-5-yl)propyl ]benzoyl]-L-glutamic acid (1), have led to the synthesis of

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