Cas 960314-89-0,(5-(benzyloxy)-1-(chloromethyl)-8-methyl-1,2-dihydrothieno[3,2-e]indol-3-yl)-(5,6,7-trimethoxyindol-2-yl)methanone

960314-89-0

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Basic information

Product Name: (5-(benzyloxy)-1-(chloromethyl)-8-methyl-1,2-dihydrothieno[3,2-e]indol-3-yl)-(5,6,7-trimethoxyindol-2-yl)methanone
Synonyms: (5-(benzyloxy)-1-(chloromethyl)-8-methyl-1,2-dihydrothieno[3,2-e]indol-3-yl)-(5,6,7-trimethoxyindol-2-yl)methanone
CAS NO:960314-89-0
Molecular Formula:
Molecular Weight: 577.101
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: (5-(benzyloxy)-1-(chloromethyl)-8-methyl-1,2-dihydrothieno[3,2-e]indol-3-yl)-(5,6,7-trimethoxyindol-2-yl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (5-(benzyloxy)-1-(chloromethyl)-8-methyl-1,2-dihydrothieno[3,2-e]indol-3-yl)-(5,6,7-trimethoxyindol-2-yl)methanone(960314-89-0)
EPA Substance Registry System: (5-(benzyloxy)-1-(chloromethyl)-8-methyl-1,2-dihydrothieno[3,2-e]indol-3-yl)-(5,6,7-trimethoxyindol-2-yl)methanone(960314-89-0)

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: 960314-89-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 960314-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,3,1 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 960314-89:
(8*9)+(7*6)+(6*0)+(5*3)+(4*1)+(3*4)+(2*8)+(1*9)=170
170 % 10 = 0
So 960314-89-0 is a valid CAS Registry Number.

960314-89-0Upstream product

128781-07-7 5,6,7-trimethoxy-1H-indole-2-carboxylic acid

960314-89-0Downstream Products

960314-89-0Relevant academic research and scientific papers

Rational design, synthesis, and evaluation of key analogues of CC-1065 and the duocarmycins

Tichenor, Mark S.,MacMillan, Karen S.,Stover, James S.,Wolkenberg, Scott E.,Pavani, Maria G.,Zanella, Lorenzo,Zaid, Abdel N.,Spalluto, Gianpiero,Rayl, Thomas J.,Hwang, Inkyu,Baraldi, Pier Giovanni,Boger, Dale L.

, p. 14092 - 14099 (2008/09/17)

The design, synthesis, and evaluation of a predictably more potent analogue of CC-1065 entailing the substitution replacement of a single skeleton atom in the alkylation subunit are disclosed and were conducted on the basis of design principles that emerg

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