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137958-57-7

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137958-57-7 Usage

Chiral alcohol compound

(S)-1-octanol

Common uses

Production of pheromones, perfumes, and other fragrance products; solvent in industrial processes

Natural occurrence

Found in fruits and flowers

Antiviral and antibacterial properties

Useful for pharmaceutical and medicinal purposes

Characteristic odor

Distinctive smell

Check Digit Verification of cas no

The CAS Registry Mumber 137958-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,9,5 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 137958-57:
(8*1)+(7*3)+(6*7)+(5*9)+(4*5)+(3*8)+(2*5)+(1*7)=177
177 % 10 = 7
So 137958-57-7 is a valid CAS Registry Number.

137958-57-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-(benzyloxy)octan-1-ol

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:137958-57-7 SDS

137958-57-7Downstream Products

137958-57-7Relevant articles and documents

Oxirane Ring-Opening with Alcohol Catalyzed by Organotin Phosphate Condensates. Complete Inversion at Tertiary and Benzylic Centers

Otera, Junzo,Niibo, Yoshihisa,Nozaki, Hitosi

, p. 7625 - 7634 (2007/10/02)

Regio- and stereospecific ring-opening of chiral oxiranes has been effected by organotin phosphate condensates catalyst.Alcohols attack on the tertiary and benzylic positions exclusively.Despite seemingly acidic character of the catalyst in terms of regioselectivity the chiral centers are completely inverted.The new methodology is applied to synthesis of enantiomerically pure linalool and to conversion of commercially available (R)-styrene oxide into the (S)-counterpart.

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