Cas 96207-22-6,7-Thia-2-azabicyclo[2.2.1]hept-5-ene-5,6-dicarboxylic acid, 1,4-diphenyl-2-(phenylmethyl)-3-thioxo-, dimethyl ester

96207-22-6

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Basic information

Product Name: 7-Thia-2-azabicyclo[2.2.1]hept-5-ene-5,6-dicarboxylic acid, 1,4-diphenyl-2-(phenylmethyl)-3-thioxo-, dimethyl ester
Synonyms:
CAS NO:96207-22-6
Molecular Formula: C28H23NO4S2
Molecular Weight: 501.627
EINECS: N/A
Product Categories: N/A
Mol File: 96207-22-6.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: 7-Thia-2-azabicyclo[2.2.1]hept-5-ene-5,6-dicarboxylic acid, 1,4-diphenyl-2-(phenylmethyl)-3-thioxo-, dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 7-Thia-2-azabicyclo[2.2.1]hept-5-ene-5,6-dicarboxylic acid, 1,4-diphenyl-2-(phenylmethyl)-3-thioxo-, dimethyl ester(96207-22-6)
EPA Substance Registry System: 7-Thia-2-azabicyclo[2.2.1]hept-5-ene-5,6-dicarboxylic acid, 1,4-diphenyl-2-(phenylmethyl)-3-thioxo-, dimethyl ester(96207-22-6)

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: 96207-22-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96207-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,0 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96207-22:
(7*9)+(6*6)+(5*2)+(4*0)+(3*7)+(2*2)+(1*2)=136
136 % 10 = 6
So 96207-22-6 is a valid CAS Registry Number.

96207-22-6Upstream product

3704-40-3 2,5-diphenyl-1,3-thiazole

96207-22-6Downstream Products

96207-22-6Relevant articles and documents

Studies on Mesoionic Compounds. XIV. Synthesis of Mesoionic 1,3-Thiazolium-4-thiolates

Takezawa, Katsushi,Nomura, Keiichi,Yoshii, Eiichi,Masuda, Katsutada

, p. 4637 - 4640 (2007/10/02)

Two approaches to 3-alkyl-2,5-diphenyl-1,3-thiazolium-4-thiolate (4) are described: (1) exchange of the exocyclic oxygen atom of the mesoionic 4-olate (6) with sulfur via O-methylation and (2) base-catalyzed thiation of the N-alkyl-1,3-thiazolium compound

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