Cas 1239607-29-4,ethyl 5-(2,6-dichlorophenyl)-7-methyl-3-oxo-3,5-dihydro-2H-thiazolo[3,2-a]pyrimidine-6-carboxylate

1239607-29-4

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Basic information

Product Name: ethyl 5-(2,6-dichlorophenyl)-7-methyl-3-oxo-3,5-dihydro-2H-thiazolo[3,2-a]pyrimidine-6-carboxylate
Synonyms:
CAS NO:1239607-29-4
Molecular Formula:
Molecular Weight: 385.271
EINECS: N/A
Product Categories: N/A

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: ethyl 5-(2,6-dichlorophenyl)-7-methyl-3-oxo-3,5-dihydro-2H-thiazolo[3,2-a]pyrimidine-6-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 5-(2,6-dichlorophenyl)-7-methyl-3-oxo-3,5-dihydro-2H-thiazolo[3,2-a]pyrimidine-6-carboxylate(1239607-29-4)
EPA Substance Registry System: ethyl 5-(2,6-dichlorophenyl)-7-methyl-3-oxo-3,5-dihydro-2H-thiazolo[3,2-a]pyrimidine-6-carboxylate(1239607-29-4)

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: 1239607-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1239607-29-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,6,0 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1239607-29:
(9*1)+(8*2)+(7*3)+(6*9)+(5*6)+(4*0)+(3*7)+(2*2)+(1*9)=164
164 % 10 = 4
So 1239607-29-4 is a valid CAS Registry Number.

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1239607-29-4Relevant academic research and scientific papers

An efficient synthesis of some novel bicyclic thiazolopyrimidine derivatives

Mobinikhaledi, Akbar,Zendehdel, Mojgan,Nasab, Mahdia Hamidi,Fard, Mohammad Ali Bodaghi

, p. 451 - 458 (2009)

An efficient and rapid synthesis of some thiazolopyrimidine derivatives from pyrimidinthiones and chloroacetyl chloride in refluxing tetrahydrofurane (THF) is described. The method is simple and practical, and generating thiazole derivatives in good isola

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