Cas 109532-74-3,1-Benzyl-2-benzylsulfanyl-6-oxo-4-thiophen-2-yl-1,6-dihydro-pyrimidine-5-carbonitrile

109532-74-3

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Basic information

Product Name: 1-Benzyl-2-benzylsulfanyl-6-oxo-4-thiophen-2-yl-1,6-dihydro-pyrimidine-5-carbonitrile
Synonyms:
CAS NO:109532-74-3
Molecular Formula:
Molecular Weight: 415.539
EINECS: N/A
Product Categories: N/A
Mol File: 109532-74-3.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: 1-Benzyl-2-benzylsulfanyl-6-oxo-4-thiophen-2-yl-1,6-dihydro-pyrimidine-5-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 1-Benzyl-2-benzylsulfanyl-6-oxo-4-thiophen-2-yl-1,6-dihydro-pyrimidine-5-carbonitrile(109532-74-3)
EPA Substance Registry System: 1-Benzyl-2-benzylsulfanyl-6-oxo-4-thiophen-2-yl-1,6-dihydro-pyrimidine-5-carbonitrile(109532-74-3)

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: 109532-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109532-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,3 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109532-74:
(8*1)+(7*0)+(6*9)+(5*5)+(4*3)+(3*2)+(2*7)+(1*4)=123
123 % 10 = 3
So 109532-74-3 is a valid CAS Registry Number.

109532-74-3Upstream product

109532-65-2 4-oxo-6-(thiophen-2-yl)-2-sulfanylidene-1,2,3,4-tetrahydropyrimidine-5-carbonitrile

109532-74-3Downstream Products

109532-74-3Relevant articles and documents

Chemotherapeutical Agents, V. - Syntheses and Activities of Novel Pyrimidines Derived from 5-Cyano-6-aryl-2-thiouracil

Ram, Vishnu J.,Berghe, Dirk A. Vanden,Vlietinck, Arnold J.

, p. 797 - 801 (2007/10/02)

The 5-cyano-6-aryl-2-thiouracils 1a-d were prepared for the syntheses of several other pyrimidine derivatives.In basic medium 1a reacted with picryl chloride yielding the unexpected benzothiazolo-pyrimidine 2.Heating a mixture of 1 and 1,2-dibromoethane i

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