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3H-Benz[e]indole-3-carboxylic acid, 1,2-dihydro-5-(phenylmethoxy)-1-[[(2,2,6,6-tetramethyl-1-piperidinyl)oxy] methyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161646-55-5

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161646-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161646-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,6,4 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 161646-55:
(8*1)+(7*6)+(6*1)+(5*6)+(4*4)+(3*6)+(2*5)+(1*5)=135
135 % 10 = 5
So 161646-55-5 is a valid CAS Registry Number.

161646-55-5Relevant academic research and scientific papers

ISOQUINOLIDINOBENZODIAZEPINE (IQB)-1(CHLOROMETHYL)-2,3-DIHYDRO-1H-BENZO[E]INDOLE (CBI) DIMERS

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Paragraph 0011; 00241; 00259-00261, (2018/04/27)

Provided herein are isoquinolidinobenzodiazepine (IQB)-1(chloromethyl)-2,3-dihydro-1H-benzo[e]indole (CBI) dimers, antibody-drug conjugates comprising them and methods of use for killing cells and treating disease.

An efficient synthesis of 1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI): An enhanced and simplified analog of the CC-1065 and duocarmycin alkylation subunits

Boger,McKie

, p. 1271 - 1275 (2007/10/02)

An efficient synthesis of 4, the immediate precursor to N-BOC-CBI and related analogs of CC-1065 incorporating the 1,2,9,9a-tetrahydrocyclopropa[c]benz[c]indol-4-one alkylation subunit, is described based on a Tempo trap of a 5-exo-trig aryl radical-alken

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