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52322-76-6

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52322-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52322-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,2 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52322-76:
(7*5)+(6*2)+(5*3)+(4*2)+(3*2)+(2*7)+(1*6)=96
96 % 10 = 6
So 52322-76-6 is a valid CAS Registry Number.

52322-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-diphenyl-3-methoxyaminopropan-1-one

1.2 Other means of identification

Product number -
Other names 3-methoxyamino-1,3-diphenyl-propan-1-one

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:52322-76-6 SDS

52322-76-6Relevant articles and documents

Exchange Processes in Shibasaki's Rare Earth Alkali Metal BINOLate Frameworks and Their Relevance in Multifunctional Asymmetric Catalysis

Robinson, Jerome R.,Gu, Jun,Carroll, Patrick J.,Schelter, Eric J.,Walsh, Patrick J.

, p. 7135 - 7144 (2015/06/25)

Shibasaki's rare earth alkali metal BINOLate (REMB) catalysts (REMB; RE = Sc, Y, La - Lu; M = Li, Na, K; B = 1,1-bi-2-naphtholate; RE/M/B = 1/3/3) are among the most successful enantioselective catalysts and have been employed in a broad range of mechanis

A novel two-step preparation of enaminoketones by amination of α,β- unsaturated ketones with methoxyamine

Seko, Shinzo,Tani, Nobuhiro

, p. 8117 - 8120 (2007/10/03)

β-Methoxyaminoketones, derived from the addition of methoxyamine to 1,3-diaryl-2-propen-1-one, underwent base-induced β-elimination to furnish the corresponding enaminoketones in good to moderate yields. The reaction conditions and substituents on the substrates significantly influenced the selectivity in the production of enaminoketone and/or aziridineketone.

3-Methoxyamino-1,3-diarylpropan-1-one und N-(N-Phenylcarbamoyl)-Derivate

Weber, Fritz Gerd,Liepert, Harald

, p. 173 - 175 (2007/10/02)

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