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116041-30-6

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116041-30-6 Usage

General Description

(R)-1-Benzyl-5-hydroxymethyl-2-pyrrolidinone is a chemical compound with potential pharmaceutical applications. It is a pyrrolidinone derivative with a hydroxyl group and a benzyl group attached to the nitrogen and carbon atoms, respectively. (R)-1-BENZYL-5-HYDROXYMETHYL-2- PYRROLIDINONE has been studied for its potential use as a chiral building block in the synthesis of biologically active molecules, such as pharmaceutical drugs and agrochemicals. It has also shown potential as a ligand in asymmetric catalytic reactions. Overall, (R)-1-Benzyl-5-hydroxymethyl-2-pyrrolidinone is a versatile chemical that has garnered interest in various fields due to its unique structural and functional properties.

Check Digit Verification of cas no

The CAS Registry Mumber 116041-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,4 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116041-30:
(8*1)+(7*1)+(6*6)+(5*0)+(4*4)+(3*1)+(2*3)+(1*0)=76
76 % 10 = 6
So 116041-30-6 is a valid CAS Registry Number.

116041-30-6SDS

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 (R)-1-BENZYL-5-HYDROXYMETHYL-2- PYRROLIDINONE

1.2 Other means of identification

Product number -
Other names 1-benzyl-2-hydroxymethyl-5-pyrrolidinone

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:116041-30-6 SDS

116041-30-6Relevant articles and documents

Rhodium-Catalyzed Stereospecific C?H Amination for the Construction of Spiroaminal Cores: Reactivity Difference between Nitrenoid and Carbenoid Species against Amide Functionality

Kono, Masato,Harada, Shingo,Nemoto, Tetsuhiro

, p. 7428 - 7432 (2017/06/06)

Metal nitrenoids and metal carbenoids exhibit similar reactivity for insertion into a C?H bond and a C=C double bond. These reactions have attracted the attention of organic chemists due to their unusual bond-forming ability, but the reactivity difference between these chemical species has not been studied. In this paper, we examined the reactivity difference using the corresponding Rh nitrenoid and Rh carbenoid precursors. The Rh nitrenoid inserted into an intramolecular C(sp3)?H bond adjacent to an amide nitrogen, affording functionalized spiroaminals that are ubiquitous in natural products, while the Rh carbenoid inserted into an amide C?N bond. The totally different reactivity was rationalized by the relatively low energy barrier for the C?H insertion reaction of the Rh nitrenoid. Computational analysis suggests that the origin of the discrepancy is the electrophilicity of the coordinating atoms to the Rh complex.

3-arylcarbonyl-1-(C-attached-N-heteryl)-1H-indoles

-

, (2008/06/13)

2-R2 -R4 -substituted-3-R3 -CO-1-[(C-attached-N-herteryl)-(Alk)n ]-1H-indoles useful as analgesic, anti-rheumatic, anti-inflammatory or anti-glaucoma agents.

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