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2-(2-bromo-4-carboxylic acid methyl ester phenoxy)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54110-86-0

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54110-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54110-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,1 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54110-86:
(7*5)+(6*4)+(5*1)+(4*1)+(3*0)+(2*8)+(1*6)=90
90 % 10 = 0
So 54110-86-0 is a valid CAS Registry Number.

54110-86-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-bromo-4-carboxylic acid methyl ester phenoxy)ethanol

1.2 Other means of identification

Product number -
Other names 2-(2-bromo-4-methoxycarbonyl-phenoxy)-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:54110-86-0 SDS

54110-86-0Relevant academic research and scientific papers

Palladium-catalyzed intramolecular C-O bond formation

Kuwabe,Torraca,Buchwald

, p. 12202 - 12206 (2007/10/03)

A number of oxygen heterocycles were synthesized using the palladium-catalyzed intramolecular etherification of aryl halides by employing di-tert-butylphosphinobiaryl ligands. The reaction proceeds under mild conditions using weak bases such as Cs2CO3 or K3PO4. A variety of functional groups are tolerated in the reaction, and enantioenriched alcohols can be coupled without erosion of optical purity. The mildness of the reaction conditions allows for the use of polyfunctionalized substrates. This method was used as the key step in the synthesis of MKC-242, an antidepressant currently in clinical trials. The synthesis of MKC-242 was achieved in 40% overall yield from commercially available sesamol and acrylonitrile.

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