Cas 132846-84-5,5-amino-2-benzoylmethylene-3-phenyl-Δ<sup>4</sup>-1,3,4-thiadiazoline hydrobromide

132846-84-5

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Basic information

Product Name: 5-amino-2-benzoylmethylene-3-phenyl-Δ⁴-1,3,4-thiadiazoline hydrobromide
Synonyms: 5-amino-2-benzoylmethylene-3-phenyl-Δ⁴-1,3,4-thiadiazoline hydrobromide
CAS NO:132846-84-5
Molecular Formula:
Molecular Weight: 376.277
EINECS: N/A
Product Categories: N/A
Mol File: 132846-84-5.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: 5-amino-2-benzoylmethylene-3-phenyl-Δ⁴-1,3,4-thiadiazoline hydrobromide(CAS DataBase Reference)
NIST Chemistry Reference: 5-amino-2-benzoylmethylene-3-phenyl-Δ⁴-1,3,4-thiadiazoline hydrobromide(132846-84-5)
EPA Substance Registry System: 5-amino-2-benzoylmethylene-3-phenyl-Δ⁴-1,3,4-thiadiazoline hydrobromide(132846-84-5)

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: 132846-84-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132846-84-5 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, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132846-84:
(8*1)+(7*3)+(6*2)+(5*8)+(4*4)+(3*6)+(2*8)+(1*4)=135
135 % 10 = 5
So 132846-84-5 is a valid CAS Registry Number.

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132846-84-5Relevant articles and documents

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 (2007/10/02)

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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