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2-Pyrrolidinone, 3,3-dichloro-4-methyl-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

358622-50-1

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358622-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358622-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,6,2 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 358622-50:
(8*3)+(7*5)+(6*8)+(5*6)+(4*2)+(3*2)+(2*5)+(1*0)=161
161 % 10 = 1
So 358622-50-1 is a valid CAS Registry Number.

358622-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-3,3-dichloro-4-methylpyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names -

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:358622-50-1 SDS

358622-50-1Downstream Products

358622-50-1Relevant academic research and scientific papers

Radical reactions using decacarbonyldimanganese under biphasic conditions

Huther, Nathalie,McGrail, P. Terry,Parsons, Andrew F.

, p. 1740 - 1749 (2007/10/03)

Radical reactions of alkyl halides, initiated by photolysis in the presence of decacarbonyldimanganese, can be performed in biphasic media. Reactions in the presence of aqueous sodium hydroxide together with a phase-transfer catalyst result in the efficient removal of manganese halide by-products and also lead to the regeneration of decacarbonyldimanganese. A range of efficient radical couplings, cyclisations and intermolecular addition reactions were performed under these conditions. This included the development of a new tandem radical addition-ionic cyclisation sequence that was employed in a short approach to (±)-coronamic acid. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

Synthesis of 5-methoxylated 3-pyrrolin-2-ones via the rearrangement of chlorinated pyrrolidin-2-ones

Ghelfi, Franco,Stevens, Christian V.,Laureyn, Inge,Van Meenen, Ellen,Rogge, Tina M.,De Buyck, Laurent,Nikitin, Kirill V.,Grandi, Romano,Libertini, Emanuela,Pagnoni, Ugo M.,Schenetti, Luisa

, p. 1147 - 1157 (2007/10/03)

The reaction of N-substituted 4-methyl-2-pyrrolidinones or 4-diethoxyphosphoryl analogues, carrying at least two chlorine atoms between the C(3) and C(6) carbons, with alkaline methoxide in methanol afforded the corresponding 5-methoxylated 3-pyrrolin-2-ones, useful adducts for the preparation of agrochemicals or medicinal compounds.

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