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74840-45-2

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74840-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74840-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,4 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74840-45:
(7*7)+(6*4)+(5*8)+(4*4)+(3*0)+(2*4)+(1*5)=142
142 % 10 = 2
So 74840-45-2 is a valid CAS Registry Number.

74840-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-methyl-2-methylthio-4-phenyl-3,4,5,6-tetrahydropyrimidine-5-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 6-methyl-4-phenyl-2-methylsulfanyl-1,6-dihydropyrimidine-5-carboxylate

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:74840-45-2 SDS

74840-45-2Relevant articles and documents

Novel pyrimidinic selenourea induces DNA damage, cell cycle arrest, and apoptosis in human breast carcinoma

Barbosa, Flavio A.R.,Siminski, Tamila,Canto, R?mulo F.S.,Almeida, Gabriela M.,Mota, Nádia S.R.S.,Ourique, Fabiana,Pedrosa, Rozangela Curi,Braga, Antonio Luiz

, p. 503 - 515 (2018/06/15)

Novel pyrimidinic selenoureas were synthesized and evaluated against tumour and normal cell lines. Among these, the compound named 3j initially showed relevant cytotoxicity and selectivity for tumour cells. Three analogues of 3j were designed and synthesi

Synthesis, molecular docking, and cardioprotective activity of 2-methylthio-1,4-dihydropyrimidines

Sawant, Ramesh L.,Sarode, Varsha I.,Jadhav, Ganesh D.,Wadekar, Jyoti B.

, p. 1825 - 1832 (2012/11/06)

A series of 2-methylthio-1,4-dihydropyrimidine derivatives (IIa-IIl) were synthesized in good yields by alkylation of 1,2,3,4-tetrahydropyrimidines (Ia-Il) with methyl iodide in the presence of pyridine. Their structures were confirmed by elemental analys

Efficient aerobic oxidative dehydrogenation of dihydropyrimidinones and dihydropyrimidines

Han, Bing,Han, Run-Feng,Ren, Yu-Wei,Duan, Xiao-Yong,Xu, Yi-Chuan,Zhang, Wei

supporting information; experimental part, p. 5615 - 5620 (2011/08/09)

4-Substituted dihydropyrimidinones and dihydropyrimidines were first efficient aerobic oxidized to the corresponding pyrimidinones and pyrimidines, respectively, in high yields by molecular oxygen in the presence of catalytic amount of N-hydroxyphthalimid

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