Cas 887572-52-3,4-hydroxy-6-oxo-1,2-diphenyl-1,6-dihydropyrimidin-5-yl diethyldithiocarbamate

887572-52-3

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Basic information

Product Name: 4-hydroxy-6-oxo-1,2-diphenyl-1,6-dihydropyrimidin-5-yl diethyldithiocarbamate
Synonyms: 4-hydroxy-6-oxo-1,2-diphenyl-1,6-dihydropyrimidin-5-yl diethyldithiocarbamate
CAS NO:887572-52-3
Molecular Formula: C21H21N3O2S2
Molecular Weight: 411.54034
EINECS: N/A
Product Categories: N/A
Mol File: 887572-52-3.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-hydroxy-6-oxo-1,2-diphenyl-1,6-dihydropyrimidin-5-yl diethyldithiocarbamate(CAS DataBase Reference)
NIST Chemistry Reference: 4-hydroxy-6-oxo-1,2-diphenyl-1,6-dihydropyrimidin-5-yl diethyldithiocarbamate(887572-52-3)
EPA Substance Registry System: 4-hydroxy-6-oxo-1,2-diphenyl-1,6-dihydropyrimidin-5-yl diethyldithiocarbamate(887572-52-3)

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: 887572-52-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 887572-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,5,7 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 887572-52:
(8*8)+(7*8)+(6*7)+(5*5)+(4*7)+(3*2)+(2*5)+(1*2)=233
233 % 10 = 3
So 887572-52-3 is a valid CAS Registry Number.

887572-52-3Upstream product

887572-52-3Downstream Products

887572-52-3Relevant articles and documents

Sulfenylation of heterocyclic 1,3-dicarbonyl systems: 4-Hydroxy-2-pyrones, 6-hydroxy-4-pyrimidones, 4-hydroxy-2-pyridones, 4-hydroxy-6-pyridazinones, and 5-hydroxy-3-pyrazolones

Schnell,Kappe

, p. 911 - 919 (2007/10/03)

Anions of enolized heteroaromatic 1,3-dicarbonyl systems, such as the title compounds 1, 9, 14, and 19, react in dimethylformamide in the presence of potassium carbonate with diaryl disulfides 2 to yield arylsulfenyl derivatives (3, 10, 15, 20). The arylt

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