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65853-80-7

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65853-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65853-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,5 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65853-80:
(7*6)+(6*5)+(5*8)+(4*5)+(3*3)+(2*8)+(1*0)=157
157 % 10 = 7
So 65853-80-7 is a valid CAS Registry Number.

65853-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[3-(2-formamidophenyl)-3-oxopropyl]acetamide

1.2 Other means of identification

Product number -
Other names 2-(3-acetamidopropionyl)formanilide

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:65853-80-7 SDS

65853-80-7Upstream product

65853-80-7Downstream Products

65853-80-7Relevant articles and documents

Oxidative coupling rearrangement product based on tryptamine skeleton and preparation method and application thereof

-

Paragraph 0019-0027, (2021/09/01)

The invention discloses an oxidative coupling rearrangement product based on a tryptamine skeleton and a preparation method and application thereof, wherein a corresponding dicarbonyl compound is obtained by oxidizing a color amine compound by using sodiu

Oxidative Cleavage Reaction of 3-Substituted Indoles Catalyzed by CuCl-Pyridine Complex under Oxygen

Tsuji, Jiro,Kezuka, Hiroaki,Takayanagi, Hiroshi,Yamamoto, Keiji

, p. 2369 - 2373 (2007/10/02)

Oxidative cleavage of 3-methylindole using a catalytic amount of copper (II) salts with added pyridine under an oxygen atmosphere was studied.Smooth cleavage of 3-methylindole took place to give 2-formamidoacetophenone in 73-80percent yield, whereas exclusive formation of a hydrate compound derived from 3,3'-dimethyl-3,3'-bi-3H-indole resulted under anaerobic conditions.Clean oxidative cleavage of N-acetyltryptamine, methyl 3-indolylacetate, and methyl 2-acetamido-3-(3-indolyl)propionate was also achieved, constituting a mimic of tryptophan-2,3-dioxygenase.

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