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1H-Isoindol-1-one, 2,3-dihydro-3,3-dimethyl-2-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50564-92-6

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50564-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50564-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,6 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50564-92:
(7*5)+(6*0)+(5*5)+(4*6)+(3*4)+(2*9)+(1*2)=116
116 % 10 = 6
So 50564-92-6 is a valid CAS Registry Number.

50564-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-3,3-dimethylisoindol-1-one

1.2 Other means of identification

Product number -
Other names 2-N-Benzyl-3,3-dimethylphthalimidin

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:50564-92-6 SDS

50564-92-6Downstream Products

50564-92-6Relevant academic research and scientific papers

Cobalt-catalyzed hydrocyanation and hydroarylation of enamines

Arai, Shigeru,Sato, Yuichi,Ito, Natsuki,Nishida, Atsushi

, (2019/11/13)

A mild, general and efficient hydrocyanation and hydroarylation of enamines catalyzed by Co(salen) complexes are described. Both reactions include regioselective C[sbnd]H bond formation of enamines, and the corresponding products are obtained in high yield. Hydroarylation critically discriminates the benzyl and benzoyl aromatic rings on nitrogen in cyclization step, and the corresponding isoindolinones including quaternary carbons are exclusively given.

Palladium-catalyzed oxidative activation of arylcyclopropanes

He, Zhi,Yudin, Andrei K.

, p. 5829 - 5832 (2007/10/03)

(Diagram presented) Palladium chloride-catalyzed intramolecular activation of electroneutral cyclopropane derivatives results in cleavage of the cyclopropane ring followed by formation of heterocyclic derivatives. Phenols, carboxylic acids, and amide groups were considered as substituents ortho to the cyclopropane ring in this catalytic activation chemistry. The regioselectivity observed in the case of amide-containing substrates was different from that of carboxylic acid-containing substrates, ruling out simple cyclopropane isomerization followed by a Wacker oxidation as the mechanistic pathway.

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