Cas 304015-71-2,tert-butyldimethylsilyl 2-{5-nitro-2-[(E)-2-phenylethenyl]-1H-imidazol-1-yl}ethyl ether

304015-71-2

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Basic information

Product Name: tert-butyldimethylsilyl 2-{5-nitro-2-[(E)-2-phenylethenyl]-1H-imidazol-1-yl}ethyl ether
Synonyms: tert-butyldimethylsilyl 2-{5-nitro-2-[(E)-2-phenylethenyl]-1H-imidazol-1-yl}ethyl ether
CAS NO:304015-71-2
Molecular Formula:
Molecular Weight: 373.527
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: tert-butyldimethylsilyl 2-{5-nitro-2-[(E)-2-phenylethenyl]-1H-imidazol-1-yl}ethyl ether(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyldimethylsilyl 2-{5-nitro-2-[(E)-2-phenylethenyl]-1H-imidazol-1-yl}ethyl ether(304015-71-2)
EPA Substance Registry System: tert-butyldimethylsilyl 2-{5-nitro-2-[(E)-2-phenylethenyl]-1H-imidazol-1-yl}ethyl ether(304015-71-2)

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: 304015-71-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 304015-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,0,1 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 304015-71:
(8*3)+(7*0)+(6*4)+(5*0)+(4*1)+(3*5)+(2*7)+(1*1)=82
82 % 10 = 2
So 304015-71-2 is a valid CAS Registry Number.

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304015-71-2Relevant academic research and scientific papers

Synthesis and Evaluation of Nitroheterocyclic Carbamate Prodrugs for Use with Nitroreductase-Mediated Gene-Directed Enzyme Prodrug Therapy

Hay, Michael P.,Anderson, Robert F.,Ferry, Dianne M.,Wilson, William R.,Denny, William A.

, p. 5533 - 5545 (2007/10/03)

A variety of nitroheterocyclic carbamate prodrugs of phenylenediamine mustard and 5-amino-1-(chloromethyl)-3-[(5,6,7-trimethoxyindol-2-yl)carbonyl]-1, 2-dihydro-3H-benz[e]indoline (aminoseco-CBI-TMI), covering a wide range of reduction potential, were pre

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