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59618-42-7

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59618-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59618-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,1 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59618-42:
(7*5)+(6*9)+(5*6)+(4*1)+(3*8)+(2*4)+(1*2)=157
157 % 10 = 7
So 59618-42-7 is a valid CAS Registry Number.

59618-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-1-methyl-5-(3-methylphenyl)pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names 5-Hydroxy-1-methyl-5-(m-tolyl)pyrrolidone

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:59618-42-7 SDS

59618-42-7Downstream Products

59618-42-7Relevant articles and documents

Synthesis of Chiral γ-Lactams via in Situ Elimination/Iridium-Catalyzed Asymmetric Hydrogenation of Racemic γ-Hydroxy γ-Lactams

Yuan, Qianjia,Liu, Delong,Zhang, Wanbin

supporting information, p. 1886 - 1889 (2017/04/11)

Chiral γ-lactams have been synthesized in excellent yields and enantioselectivities (up to 99% yield and 96% ee) from easily accessible racemic γ-hydroxy γ-lactams via an iridium-phosphoramidite catalyzed asymmetric hydrogenation. The reaction was designed based on insight into the reaction mechanism demonstrated in previous work and can be carried out at a reduced catalyst loading of 0.1 mol % on a gram scale. Several potential bioactive compounds can be synthesized from the reduced products. Mechanistic studies indicated that the reduced products were obtained via the hydrogenation of the N-acyliminium cations, generated from γ-hydroxy γ-lactams.

5-Hydroxy-5-substituted phenyl-pyrrolidones and piperidinones

-

, (2008/06/13)

5-hydroxy-5-substituted phenyl-pyrrolidones and piperidinones, 3.g., 5-hydroxy-1-methyl-5-(m-trifluoromethylphenyl)pyrrolidone, are useful as sedative-hypnotic agents and minor tranquilizers.

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