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1051316-41-6

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1051316-41-6 Usage

General Description

(R)-4-Hydroxy-piperidin-2-one, also known as (R)-4-hydroxy-2-pyrrolidinone, is a chemical compound with a molecular formula C5H9NO2. It is a cyclic amino acid derivative that contains a piperidin-2-one moiety with a hydroxy substituent at the fourth position. (R)-4-HYDROXY-PIPERIDIN-2-ONE is used as a key intermediate in the synthesis of various pharmaceutical and agricultural products, such as antiviral and antitumor agents. It also has potential applications in organic synthesis and as a building block in the creation of novel chemical compounds. Studies have shown that (R)-4-hydroxy-piperidin-2-one exhibits antioxidant and anti-inflammatory properties, making it a compound of interest in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1051316-41-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,1,3,1 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1051316-41:
(9*1)+(8*0)+(7*5)+(6*1)+(5*3)+(4*1)+(3*6)+(2*4)+(1*1)=96
96 % 10 = 6
So 1051316-41-6 is a valid CAS Registry Number.

1051316-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-4-hydroxypiperidin-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

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More Details:1051316-41-6 SDS

1051316-41-6Relevant articles and documents

Synthesis of both enantiomers of the Streptomyces alkaloid 4-epi-SS20846A

Scarpi, Dina,Avataneo, Ottavia,Prandi, Cristina,Venturello, Paolo,Occhiato, Ernesto G.

, p. 3688 - 3692 (2012)

The enantiodivergent synthesis of the Streptomyces alkaloid 4-epi-SS20846A was based on a Takai olefination/Suzuki-Miyaura coupling sequence for the highly stereoselective introduction of the E,E-pentadienyl side chain on the piperidine skeleton. Optical

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