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Cyclopentanone, 3-hydroxy-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109905-53-5

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109905-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109905-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,0 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109905-53:
(8*1)+(7*0)+(6*9)+(5*9)+(4*0)+(3*5)+(2*5)+(1*3)=135
135 % 10 = 5
So 109905-53-5 is a valid CAS Registry Number.

109905-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-3-hydroxycyclopentanone

1.2 Other means of identification

Product number -
Other names (R)-3-Hydroxy-cyclopentanone

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:109905-53-5 SDS

109905-53-5Upstream product

109905-53-5Downstream Products

109905-53-5Relevant academic research and scientific papers

Enantioselective Michael addition of water

Chen, Bi-Shuang,Resch, Verena,Otten, Linda G.,Hanefeld, Ulf

, p. 3020 - 3030 (2015/02/05)

The enantioselective Michael addition using water as both nucleophile and solvent has to date proved beyond the ability of synthetic chemists. Herein, the direct, enantioselective Michael addition of water in water to prepare important β-hydroxy carbonyl compounds using whole cells of Rhodococcus strains is described. Good yields and excellent enantioselectivities were achieved with this method. Deuterium labeling studies demonstrate that a Michael hydratase catalyzes the water addition exclusively with anti-stereochemistry.

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