Cas 929600-92-0,5-Pyrimidinecarbothioic acid, 1,2,3,4-tetrahydro-6-methyl-2-oxo-4-[2-(trifluoromethyl)phenyl]-, S-ethyl ester

929600-92-0

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Basic information

Product Name: 5-Pyrimidinecarbothioic acid, 1,2,3,4-tetrahydro-6-methyl-2-oxo-4-[2-(trifluoromethyl)phenyl]-, S-ethyl ester
Synonyms:
CAS NO:929600-92-0
Molecular Formula: C15H15F3N2O2S
Molecular Weight: 344.358
EINECS: N/A
Product Categories: N/A
Mol File: 929600-92-0.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-Pyrimidinecarbothioic acid, 1,2,3,4-tetrahydro-6-methyl-2-oxo-4-[2-(trifluoromethyl)phenyl]-, S-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-Pyrimidinecarbothioic acid, 1,2,3,4-tetrahydro-6-methyl-2-oxo-4-[2-(trifluoromethyl)phenyl]-, S-ethyl ester(929600-92-0)
EPA Substance Registry System: 5-Pyrimidinecarbothioic acid, 1,2,3,4-tetrahydro-6-methyl-2-oxo-4-[2-(trifluoromethyl)phenyl]-, S-ethyl ester(929600-92-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 929600-92-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 929600-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,6,0 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 929600-92:
(8*9)+(7*2)+(6*9)+(5*6)+(4*0)+(3*0)+(2*9)+(1*2)=190
190 % 10 = 0
So 929600-92-0 is a valid CAS Registry Number.

929600-92-0Upstream product

929600-92-0Downstream Products

929600-92-0Relevant articles and documents

Synthesis of 5-aroyldihydropyrimidinones via Liebeskind-Srogl thiol ester-boronic acid cross-couplings

Prokopcová, Hana,Pisani, Leonardo,Kappe, C. Oliver

, p. 43 - 46 (2007)

A novel and efficient two-step synthesis of 5-aroyl-3,4-dihydropyrimidin-2- ones is reported. These privileged ketone structures are readily generated by microwave-assisted Liebeskind-Srogl-type coupling of boronic acids with the corresponding pyrimidone

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