Cas 75615-28-0,5-nitro-1-[(2E)-3-phenylprop-2-enoyl]-1H-benzotriazole

75615-28-0

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Basic information

Product Name: 5-nitro-1-[(2E)-3-phenylprop-2-enoyl]-1H-benzotriazole
Synonyms: 1H-Benzotriazole, 5-nitro-1-(1-oxo-3-phenyl-2-propenyl)-
CAS NO:75615-28-0
Molecular Formula: C₁₅H₁₀N₄O₃
Molecular Weight: 294.2649
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 533.1°C at 760 mmHg
Flash Point: 276.2°C
Appearance: N/A
Density: 1.39g/cm³
Vapor Pressure: 1.92E-11mmHg at 25°C
Refractive Index: 1.687
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-nitro-1-[(2E)-3-phenylprop-2-enoyl]-1H-benzotriazole(CAS DataBase Reference)
NIST Chemistry Reference: 5-nitro-1-[(2E)-3-phenylprop-2-enoyl]-1H-benzotriazole(75615-28-0)
EPA Substance Registry System: 5-nitro-1-[(2E)-3-phenylprop-2-enoyl]-1H-benzotriazole(75615-28-0)

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: 75615-28-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75615-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,1 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75615-28:
(7*7)+(6*5)+(5*6)+(4*1)+(3*5)+(2*2)+(1*8)=140
140 % 10 = 0
So 75615-28-0 is a valid CAS Registry Number.

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75615-28-0Relevant academic research and scientific papers

1-Aroyl-5-nitrobenzotriazole. 6. Antiinflammatory agents

Kreutzberger,Stratmann

, p. 1250 - 1252 (2007/10/02)

Based on the concept of the anellated heterocycle as the common structural characteristic of a series of antiinflammatory agents, 5-nitrobenzotriazole (1) was caused to react with cinnamoyl chloride (2a) and 4-fluorobenzoyl chloride (2b). The structure of the end products 1-cinnamoyl-5-nitrobenzotriazole (3a) and 1-(4-fluorobenzoyl)-5-nitrobenzotriazole (3b) is supported spectroscopically. 3a exhibits marked antiinflammatory activity.

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