Cas 1092563-20-6,N-(4-(2-cyanoacetyl)-5-oxo-5,6-dihydro-4H-1,3,4-thiadiazin-2-yl)benzamide

1092563-20-6

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Basic information

Product Name: N-(4-(2-cyanoacetyl)-5-oxo-5,6-dihydro-4H-1,3,4-thiadiazin-2-yl)benzamide
Synonyms: N-(4-(2-cyanoacetyl)-5-oxo-5,6-dihydro-4H-1,3,4-thiadiazin-2-yl)benzamide
CAS NO:1092563-20-6
Molecular Formula:
Molecular Weight: 302.313
EINECS: N/A
Product Categories: N/A
Mol File: 1092563-20-6.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: N-(4-(2-cyanoacetyl)-5-oxo-5,6-dihydro-4H-1,3,4-thiadiazin-2-yl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-(2-cyanoacetyl)-5-oxo-5,6-dihydro-4H-1,3,4-thiadiazin-2-yl)benzamide(1092563-20-6)
EPA Substance Registry System: N-(4-(2-cyanoacetyl)-5-oxo-5,6-dihydro-4H-1,3,4-thiadiazin-2-yl)benzamide(1092563-20-6)

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: 1092563-20-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1092563-20-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,5,6 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1092563-20:
(9*1)+(8*0)+(7*9)+(6*2)+(5*5)+(4*6)+(3*3)+(2*2)+(1*0)=146
146 % 10 = 6
So 1092563-20-6 is a valid CAS Registry Number.

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1092563-20-6Relevant articles and documents

Heterocyclic synthesis with 4-benzoyl-1-cyanoacetylthiosemicarbazide: Selective synthesis of some thiazole, triazole, thiadiazine, pyrrylthiazole, and pyrazolo[1,5-a]triazine derivatives

Bondock, Samir,El-Gaber Tarhoni, Abd,Fadda, Ahmed A.

, p. 153 - 159 (2008)

4-Benzoyl-1-cyanoacetylthiosemicarbazide undergoes coupling reaction with aromatic diazonium chloride to afford (arylhydrazono)thiosemicarbazide, which was reacted with phenacyl bromide regioselectivity to afford the thiazoline. The (arylhydrazono)thiosem

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