Cas 1415040-91-3,1-[5-(4-methylphenylamino)-1,2,3-thiadiazol-4-yl]ethanethione

1415040-91-3

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Basic information

Product Name: 1-[5-(4-methylphenylamino)-1,2,3-thiadiazol-4-yl]ethanethione
Synonyms: 1-[5-(4-methylphenylamino)-1,2,3-thiadiazol-4-yl]ethanethione
CAS NO:1415040-91-3
Molecular Formula:
Molecular Weight: 249.36
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-[5-(4-methylphenylamino)-1,2,3-thiadiazol-4-yl]ethanethione(CAS DataBase Reference)
NIST Chemistry Reference: 1-[5-(4-methylphenylamino)-1,2,3-thiadiazol-4-yl]ethanethione(1415040-91-3)
EPA Substance Registry System: 1-[5-(4-methylphenylamino)-1,2,3-thiadiazol-4-yl]ethanethione(1415040-91-3)

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: 1415040-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415040-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,0,4 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1415040-91:
(9*1)+(8*4)+(7*1)+(6*5)+(5*0)+(4*4)+(3*0)+(2*9)+(1*1)=113
113 % 10 = 3
So 1415040-91-3 is a valid CAS Registry Number.

1415040-91-3Upstream product

1415041-14-3 5-methyl-N-(4-methylphenyl)-1,2,3-thiadiazole-4-carboxamide

1415040-91-3Downstream Products

1415040-91-3Relevant academic research and scientific papers

Synthesis of 4-thioacetyl-1,2,3-thiadiazoles. Reversible rearrangement of N-substituted 5-methyl-1,2,3-thiadiazole-4-carbothioamides

Prokhorova,Kalinina,Glukhareva,Morzherin, Yu. Yu.

, p. 1333 - 1336 (2013/02/22)

The equilibrium in the reversible rearrangement of 5-methyl-1,2,3- thiadiazole-4-carbothioamides into 5-amino-4-thioacetyl-1,2,3-thiadiazoles is displaced toward the former, and polar solvents favor increased fraction of the thioketone. Pleiades Publishin

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