Cas 78959-02-1,2-[2-(2-Iodo-benzoylamino)-1-phenyl-2-thioxo-ethylidene]-[1,3]dithiole-4,5-dicarboxylic acid diethyl ester

78959-02-1

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Basic information

Product Name: 2-[2-(2-Iodo-benzoylamino)-1-phenyl-2-thioxo-ethylidene]-[1,3]dithiole-4,5-dicarboxylic acid diethyl ester
Synonyms: 2-[2-(2-Iodo-benzoylamino)-1-phenyl-2-thioxo-ethylidene]-[1,3]dithiole-4,5-dicarboxylic acid diethyl ester
CAS NO:78959-02-1
Molecular Formula:
Molecular Weight: 625.529
EINECS: N/A
Product Categories: N/A
Mol File: 78959-02-1.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: 2-[2-(2-Iodo-benzoylamino)-1-phenyl-2-thioxo-ethylidene]-[1,3]dithiole-4,5-dicarboxylic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[2-(2-Iodo-benzoylamino)-1-phenyl-2-thioxo-ethylidene]-[1,3]dithiole-4,5-dicarboxylic acid diethyl ester(78959-02-1)
EPA Substance Registry System: 2-[2-(2-Iodo-benzoylamino)-1-phenyl-2-thioxo-ethylidene]-[1,3]dithiole-4,5-dicarboxylic acid diethyl ester(78959-02-1)

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: 78959-02-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78959-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,5 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78959-02:
(7*7)+(6*8)+(5*9)+(4*5)+(3*9)+(2*0)+(1*2)=191
191 % 10 = 1
So 78959-02-1 is a valid CAS Registry Number.

78959-02-1Upstream product

762-21-0 acetylenedicarboxylic acid diethyl ester

78959-02-1Downstream Products

82491-22-3 diethyl 2-<4-oxo-4H-1,3-benzothiazin-2-yl(phenyl)methylene>-1,3-dithiole-4,5-dicarboxylate

78959-02-1Relevant articles and documents

Studies of Heterocyclic Chemistry. Part 25. Intramolecular Cyclizations of N-Acylarylethanethioamides leading to Thiazoles, 4H-1,3-Thiazines, 4H-Pyrido-1,3-thiazines, and 4H-1,3-Benzothiazines

Nishiwaki, Tarozaemon,Kawamura, Etsuko,Abe, Noritaka,Sasaoka, Yoshiro,Kochi, Hirafumi,et al.

, p. 1239 - 1244 (2007/10/02)

Thiazoles, 4H-1,3-thiazines, 4H-pyrido-1,3-thiazines, and 4H-1,3-benzothiazines have been synthesized from N-acyl-(1,3-dithiol-2-ylidene)arylethanethioamides derived from the reactions of 4-aryl-3-halogenoacylthio-4-aryl-3-(2-halogenonicotinoylthio

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