Cas 1333242-09-3,(E)-1-(1-(chloromethyl)-5-nitro-1H-benzo[e]indol-3(2H)-yl)-3-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one

1333242-09-3

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Basic information

Product Name: (E)-1-(1-(chloromethyl)-5-nitro-1H-benzo[e]indol-3(2H)-yl)-3-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one
Synonyms: (E)-1-(1-(chloromethyl)-5-nitro-1H-benzo[e]indol-3(2H)-yl)-3-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one
CAS NO:1333242-09-3
Molecular Formula:
Molecular Weight: 438.867
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: (E)-1-(1-(chloromethyl)-5-nitro-1H-benzo[e]indol-3(2H)-yl)-3-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-(1-(chloromethyl)-5-nitro-1H-benzo[e]indol-3(2H)-yl)-3-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one(1333242-09-3)
EPA Substance Registry System: (E)-1-(1-(chloromethyl)-5-nitro-1H-benzo[e]indol-3(2H)-yl)-3-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one(1333242-09-3)

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: 1333242-09-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333242-09-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,4 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1333242-09:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*4)+(3*2)+(2*0)+(1*9)=113
113 % 10 = 3
So 1333242-09-3 is a valid CAS Registry Number.

1333242-09-3Upstream product

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1333242-09-3Relevant academic research and scientific papers

The effect of sulfonate leaving groups on the hypoxia-selective toxicity of nitro analogs of the duocarmycins

Ashoorzadeh, Amir,Atwell, Graham J.,Pruijn, Frederik B.,Wilson, William R.,Tercel, Moana,Denny, William A.,Stevenson, Ralph J.

, p. 4851 - 4860 (2011)

A series of 3-substituted (5-nitro-2,3-dihydro-1H-benzo[e]indol-1-yl)methyl sulfonate (nitroCBI) prodrugs containing sulfonate leaving groups undergo hypoxia-selective metabolism to form potent DNA minor groove alkylating agents. They were evaluated (alon

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