Cas 223138-88-3,1-[benzoylmethylsulphido-phenylaminocarbonyl]-4-(p-tolyl)-3-thiosemicarbazone

223138-88-3

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Basic information

Product Name: 1-[benzoylmethylsulphido-phenylaminocarbonyl]-4-(p-tolyl)-3-thiosemicarbazone
Synonyms: 1-[benzoylmethylsulphido-phenylaminocarbonyl]-4-(p-tolyl)-3-thiosemicarbazone
CAS NO:223138-88-3
Molecular Formula:
Molecular Weight: 434.586
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-[benzoylmethylsulphido-phenylaminocarbonyl]-4-(p-tolyl)-3-thiosemicarbazone(CAS DataBase Reference)
NIST Chemistry Reference: 1-[benzoylmethylsulphido-phenylaminocarbonyl]-4-(p-tolyl)-3-thiosemicarbazone(223138-88-3)
EPA Substance Registry System: 1-[benzoylmethylsulphido-phenylaminocarbonyl]-4-(p-tolyl)-3-thiosemicarbazone(223138-88-3)

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: 223138-88-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 223138-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,1,3 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 223138-88:
(8*2)+(7*2)+(6*3)+(5*1)+(4*3)+(3*8)+(2*8)+(1*8)=113
113 % 10 = 3
So 223138-88-3 is a valid CAS Registry Number.

223138-88-3Upstream product

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223138-88-3Relevant academic research and scientific papers

Reaction of 4-aryl-3-thiosemicarbazides with phenylisothiocyanate: A facile synthesis of thiazole, pyrazole and pyrimidine derivatives

Wardakhan, Wagnat W.,Fleita, Daisy H.,Mohareb, Rafat M.

, p. 97 - 104 (1999)

The reaction of 4-aryl-3-thiosemicarbazides 1a-d with phenylisothiocyanate gave the intermediate potasium salts 2a-d. The latter afforded 3a-d, 13a-d and 19 upon the reaction with phenacyl bromide, monochloroacetic acid and ethyl bromocyanoacetate respectively.

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