Cas 1420034-63-4,1-(3-butyl-7-methCompound No<sub>.</sub>I-511yl-5-(p-tolyl)-5H-thiazolo[3,2-a]pyrimidin-6-yl)ethanone

1420034-63-4

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Basic information

Product Name: 1-(3-butyl-7-methCompound No_.I-511yl-5-(p-tolyl)-5H-thiazolo[3,2-a]pyrimidin-6-yl)ethanone
Synonyms: 1-(3-butyl-7-methCompound No_.I-511yl-5-(p-tolyl)-5H-thiazolo[3,2-a]pyrimidin-6-yl)ethanone
CAS NO:1420034-63-4
Molecular Formula:
Molecular Weight: 356.489
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: 1-(3-butyl-7-methCompound No_.I-511yl-5-(p-tolyl)-5H-thiazolo[3,2-a]pyrimidin-6-yl)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3-butyl-7-methCompound No_.I-511yl-5-(p-tolyl)-5H-thiazolo[3,2-a]pyrimidin-6-yl)ethanone(1420034-63-4)
EPA Substance Registry System: 1-(3-butyl-7-methCompound No_.I-511yl-5-(p-tolyl)-5H-thiazolo[3,2-a]pyrimidin-6-yl)ethanone(1420034-63-4)

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: 1420034-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1420034-63-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,0,0,3 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1420034-63:
(9*1)+(8*4)+(7*2)+(6*0)+(5*0)+(4*3)+(3*4)+(2*6)+(1*3)=94
94 % 10 = 4
So 1420034-63-4 is a valid CAS Registry Number.

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1420034-63-4Relevant academic research and scientific papers

New synthesis of 3,5-disubstituted-5H-thiazolo[3,2-a]pyrimidine via ring annulation of 3,4-dihydropyrimidin-2(1H)-thione using alkynyl(aryl)iodonium salts

Shelke, Amol V.,Bhong, Bhagyashree Y.,Karade, Nandkishor N.

, p. 600 - 603 (2013)

A transition metal-free protocol for the synthesis of biologically active thiazolo[3,2-a]pyrimidine derivatives has been achieved by the cyclocondensation of 3,4-dihydropyrimidin-2(1H)-thiones with alkynyl(aryl)iodonium tosylates. This reaction demonstrat

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