Cas 87102-28-1,(E)-2-[4,6-Bis-(4-chloro-phenyl)-1,4,5,6-tetrahydro-[1,3,5]triazin-2-ylsulfanyl]-1-phenyl-ethenol

87102-28-1

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Basic information

Product Name: (E)-2-[4,6-Bis-(4-chloro-phenyl)-1,4,5,6-tetrahydro-[1,3,5]triazin-2-ylsulfanyl]-1-phenyl-ethenol
Synonyms: (E)-2-[4,6-Bis-(4-chloro-phenyl)-1,4,5,6-tetrahydro-[1,3,5]triazin-2-ylsulfanyl]-1-phenyl-ethenol
CAS NO:87102-28-1
Molecular Formula:
Molecular Weight: 456.395
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: (E)-2-[4,6-Bis-(4-chloro-phenyl)-1,4,5,6-tetrahydro-[1,3,5]triazin-2-ylsulfanyl]-1-phenyl-ethenol(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-[4,6-Bis-(4-chloro-phenyl)-1,4,5,6-tetrahydro-[1,3,5]triazin-2-ylsulfanyl]-1-phenyl-ethenol(87102-28-1)
EPA Substance Registry System: (E)-2-[4,6-Bis-(4-chloro-phenyl)-1,4,5,6-tetrahydro-[1,3,5]triazin-2-ylsulfanyl]-1-phenyl-ethenol(87102-28-1)

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: 87102-28-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87102-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,0 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87102-28:
(7*8)+(6*7)+(5*1)+(4*0)+(3*2)+(2*2)+(1*8)=121
121 % 10 = 1
So 87102-28-1 is a valid CAS Registry Number.

87102-28-1Upstream product

87102-28-1Downstream Products

87114-29-2 2,4-Bis-(4-chloro-phenyl)-6-phenyl-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazine

87102-28-1Relevant academic research and scientific papers

Reaction of 4,6-Diarylhexahydro-1,3,5-triazine-2-thiones with α-Haloketones. 3

Soliman, Adly Abdel-Wahid

, p. 99 - 101 (1984)

4,6-Diarylhexahydro-s-triazine-2-thiones reacted with α-haloketones to give the S-substituted derivatives, which were cyclized to substituted thiazolo-s-triazines. 7-(3-Aryl-2-propenoyl)-6-methyl-2,4-diphenyl-2,3,4-trihydrothiazolo-s-triazin

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