Cas 109532-83-4,1-Butyl-2-butylsulfanyl-4-(4-dimethylamino-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carbonitrile

109532-83-4

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Basic information

Product Name: 1-Butyl-2-butylsulfanyl-4-(4-dimethylamino-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carbonitrile
Synonyms:
CAS NO:109532-83-4
Molecular Formula:
Molecular Weight: 384.546
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-Butyl-2-butylsulfanyl-4-(4-dimethylamino-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 1-Butyl-2-butylsulfanyl-4-(4-dimethylamino-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carbonitrile(109532-83-4)
EPA Substance Registry System: 1-Butyl-2-butylsulfanyl-4-(4-dimethylamino-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carbonitrile(109532-83-4)

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: 109532-83-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109532-83-4 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, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109532-83:
(8*1)+(7*0)+(6*9)+(5*5)+(4*3)+(3*2)+(2*8)+(1*3)=124
124 % 10 = 4
So 109532-83-4 is a valid CAS Registry Number.

109532-83-4Upstream product

70638-55-0 6-(4-(dimethylamino)phenyl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile

109532-83-4Downstream Products

109532-83-4Relevant academic research and scientific papers

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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