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

85554-14-9

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85554-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85554-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,5 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85554-14:
(7*8)+(6*5)+(5*5)+(4*5)+(3*4)+(2*1)+(1*4)=149
149 % 10 = 9
So 85554-14-9 is a valid CAS Registry Number.

85554-14-9SDS

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 (R)-2-bromo-1-(2-naphthyl)ethanol

1.2 Other means of identification

Product number -
Other names (R)-2-Bromo-1-naphthalen-2-yl-ethanol

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:85554-14-9 SDS

85554-14-9Downstream Products

85554-14-9Relevant academic research and scientific papers

Chiral guanidine catalyzed acylative kinetic resolution of racemic 2-bromo-1-arylethanols

Sawada, Erika,Nakata, Kenya

supporting information, p. 371 - 373 (2021/03/16)

In this study, chiral guanidine catalyzed acylative kinetic resolution of racemic 2-bromo-1-arylethanols was achieved with high selectivity. Irrespective of the electronic nature and the substitution patterns on the aromatic rings, a variety of substrates were suitable for this reaction. The branched acyl component was considered to be optimal for obtaining high s-values. The transition state of the reaction was proposed based on the absolute configuration of the obtained product.

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