Cas 132846-90-3,2-(5-Phenylamino-[1,3,4]thiadiazol-2-yl)-1-thiophen-2-yl-ethanone; hydrobromide

132846-90-3

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Basic information

Product Name: 2-(5-Phenylamino-[1,3,4]thiadiazol-2-yl)-1-thiophen-2-yl-ethanone; hydrobromide
Synonyms: 2-(5-Phenylamino-[1,3,4]thiadiazol-2-yl)-1-thiophen-2-yl-ethanone; hydrobromide
CAS NO:132846-90-3
Molecular Formula:
Molecular Weight: 382.305
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: 2-(5-Phenylamino-[1,3,4]thiadiazol-2-yl)-1-thiophen-2-yl-ethanone; hydrobromide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(5-Phenylamino-[1,3,4]thiadiazol-2-yl)-1-thiophen-2-yl-ethanone; hydrobromide(132846-90-3)
EPA Substance Registry System: 2-(5-Phenylamino-[1,3,4]thiadiazol-2-yl)-1-thiophen-2-yl-ethanone; hydrobromide(132846-90-3)

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: 132846-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132846-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,4 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132846-90:
(8*1)+(7*3)+(6*2)+(5*8)+(4*4)+(3*6)+(2*9)+(1*0)=133
133 % 10 = 3
So 132846-90-3 is a valid CAS Registry Number.

132846-90-3Upstream product

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132846-90-3Relevant academic research and scientific papers

SYNTHESIS OF 1,3,4-THIADIAZOLE DERIVATIVES BY THE REACTION OF THIOSEMICARBAZIDE OR ITS 1- OR 4-SUBSTITUTED DERIVATIVES WITH SOME 1-BROMO-2-ACYLACETYLENES

Nakhmanovich, A. S.,Glotova, T. E.,Komarova, T. N.,Sigalov, M. V.,Romanenko, L. S.

, p. 1186 - 1188 (1990)

The reaction of thiosemicarbazide, 4-methyl-, 4-phenyl-, or 1-phenylthiosemicarbazides with 1-bromo-2-benzoyl(thenoyl-2)acetylenes in acetonitrile or glacial acetic acid yielded 2-acylmethylene- and 2-acylmethyl-5-amino-1,3,4-thiadiazoles.Heating of the l

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