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7-methyl-3-(4-methylphenyl)-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23429-89-2

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23429-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23429-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,2 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23429-89:
(7*2)+(6*3)+(5*4)+(4*2)+(3*9)+(2*8)+(1*9)=112
112 % 10 = 2
So 23429-89-2 is a valid CAS Registry Number.

23429-89-2SDS

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 7-methyl-3-(4-methylphenyl)-[1,3]thiazolo[3,2-a]pyrimidin-5-one

1.2 Other means of identification

Product number -
Other names 7-methyl-3-p-tolyl-thiazolo[3,2-a]pyrimidin-5-one

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:23429-89-2 SDS

23429-89-2Downstream Products

23429-89-2Relevant academic research and scientific papers

5 H - thiazolo [3, 2 - a] pyrimidine - 5 - ketone derivative and its preparation method and used as antibacterial medicament application

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Paragraph 0042; 0084; 0085; 0089; 0090, (2017/08/23)

The invention discloses 5H-thiazolo[3,2-a]pyrimidyl-5-one derivatives which have a definite chemical structure and are simple in chemical structure. The invention also discloses a preparation method of the 5H-thiazolo[3,2-a]pyrimidyl-5-one derivatives, wh

Synthesis of some new thiazolo[3,2-A]pyrimidine derivatives and screening of their in vitro antibacterial and antitubercular activities

Cai, Dong,Zhang, Zhi-Hua,Chen, Yu,Yan, Xin-Jia,Zhang, Shi-Ti,Zou, Liang-Jing,Meng, Li-Hong,Li, Fang,Fu, Bing-Jie

, p. 292 - 302 (2016/01/25)

The novel 5H-thiazolo[3,2-A]pyrimidin-5-ones were synthesized by thiophene ring closure. The first step is the synthesis of S-alkylated derivatives by the reaction of 6-substituted-2-thiouracils with the appropriate substituted phenacyl halides. Upon trea

The Chemistry of Pyrimidinethiols. II. The Preparation and Reaction of Some 2-Arenecarbonylmethylthiopyrimidines

Hurst, Derek T.,Beaumont, Claire,Jones, Derek T. E.,Kingsley, Deborah A.,Partridge, Julian D.,Rutherford, Trevor J.

, p. 1209 - 1219 (2007/10/02)

A number of 2-arenecarbonylmethylthiopyrimidin-4(1H)-ones has been synthesized.Those having H, Me or Pr as a 6-substituent undergo ready sulfur extrusion on heating in diphenyl ether to give 2-(arenecarbonylmethylene)-2,3-dihydropyrimidin-4(1H)-ones, but

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