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

61559-29-3

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61559-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61559-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,5 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61559-29:
(7*6)+(6*1)+(5*5)+(4*5)+(3*9)+(2*2)+(1*9)=133
133 % 10 = 3
So 61559-29-3 is a valid CAS Registry Number.

61559-29-3SDS

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)-(-)-4-octanol

1.2 Other means of identification

Product number -
Other names (R)-4-Octanol

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:61559-29-3 SDS

61559-29-3Upstream product

61559-29-3Downstream Products

61559-29-3Relevant academic research and scientific papers

Biocatalytic Racemization Employing TeSADH: Substrate Scope and Organic Solvent Compatibility for Dynamic Kinetic Resolution

Pop?oński, Jaros?aw,Reiter, Tamara,Kroutil, Wolfgang

, p. 763 - 768 (2018/02/27)

Racemization in combination with a kinetic resolution is the base for a dynamic kinetic resolution (DKR). Biocatalytic racemization was successfully performed for a broad scope of sec-alcohols by employing a single alcohol dehydrogenase (ADH) variant from Thermoanaerobacter pseudoethanolicus (formerly T. ethanolicus; TeSADH W110A I86A C295A). The catalyst employed as a lyophilized whole cell preparation or cell free extract, which tolerated various non-water miscible organic solvents under micro-aqueous or two-phase conditions, whereby cyclohexane and n-hexane suited best. Various concepts for combining the enzymatic racemization with an enzymatic kinetic resolution to achieve overall a bis-enzymatic DKR were evaluated. A proof of concept showed a successful DKR with racemization in aqueous phase combined with acylation in the organic phase.

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