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1H-Indole, 2-[[3-(1-hydroxyethyl)-4-pyridinyl]carbonyl]-1-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65112-68-7

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65112-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65112-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,1 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65112-68:
(7*6)+(6*5)+(5*1)+(4*1)+(3*2)+(2*6)+(1*8)=107
107 % 10 = 7
So 65112-68-7 is a valid CAS Registry Number.

65112-68-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(benzenesulfonyl)indol-2-yl]-[3-(1-hydroxyethyl)pyridin-4-yl]methanone

1.2 Other means of identification

Product number -
Other names 1-benzenesulfonyl-2-[3-(1-hydroxy-ethyl)-isonicotinoyl]-indole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65112-68-7 SDS

65112-68-7Downstream Products

65112-68-7Relevant academic research and scientific papers

Indole β-Nucleophilic Substitution. Part 2. Formation of a Benzoxepinoindole and a Pyridooxepinoindole

Cooper, Melanie M.,Hignett, Geoffrey J.,Joule, John A.

, p. 3008 - 3011 (1981)

The synthesis are described of benzoxepinoindol-11(6H,12H)-one, (12a) and 12-methylpyridooxepinoindol-5(6H,12H)-one, (5), by sequences involving the first examples of intramolecular nucleophilic substitution at an indole β-position, with departure of phenylsulphinate as leaving group from nitrogen.The spectroscopic and chemical evidence supporting the structures for these new heterocyclic systems, and thus by implication the operation of indole β-nucleophilic substitution, are detailed.

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