Cas 1355199-22-2,2-(2-oxo-2-(3-phenyl-5-thioxo-1H-1,2,4-triazol-4(5H)-yl)propan-2-yl)isoindoline-1,3-dione

1355199-22-2

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Basic information

Product Name: 2-(2-oxo-2-(3-phenyl-5-thioxo-1H-1,2,4-triazol-4(5H)-yl)propan-2-yl)isoindoline-1,3-dione
Synonyms: 2-(2-oxo-2-(3-phenyl-5-thioxo-1H-1,2,4-triazol-4(5H)-yl)propan-2-yl)isoindoline-1,3-dione
CAS NO:1355199-22-2
Molecular Formula:
Molecular Weight: 378.411
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-(2-oxo-2-(3-phenyl-5-thioxo-1H-1,2,4-triazol-4(5H)-yl)propan-2-yl)isoindoline-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-oxo-2-(3-phenyl-5-thioxo-1H-1,2,4-triazol-4(5H)-yl)propan-2-yl)isoindoline-1,3-dione(1355199-22-2)
EPA Substance Registry System: 2-(2-oxo-2-(3-phenyl-5-thioxo-1H-1,2,4-triazol-4(5H)-yl)propan-2-yl)isoindoline-1,3-dione(1355199-22-2)

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: 1355199-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1355199-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,1,9 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1355199-22:
(9*1)+(8*3)+(7*5)+(6*5)+(5*1)+(4*9)+(3*9)+(2*2)+(1*2)=172
172 % 10 = 2
So 1355199-22-2 is a valid CAS Registry Number.

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1355199-22-2Relevant academic research and scientific papers

Utility of phthalimidoacyl isothiocyanate in synthesis of quinazolines, benzoxazoles, benzimidazoles, 1,2,4-triazoles, and oxatriazepines

Hemdan,Fahmy,Aly,Hegazi,El-Sayed

, p. 181 - 189 (2012/02/16)

Phthalimidoacyl isothiocyanates 1a,b participated in a wide range of addition-cyclization reactions. Simultaneous or subsequent cyclization of the obtained adducts gave derivatives of quinazoline, benzoxazole, benzimidazole, 1,2,4-triazole, and oxatriazepine. The structures of all the products were confirmed by microanalytical and spectroscopic data.

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