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111000-54-5

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111000-54-5 Usage

Physical state

colorless liquid

Odor

pungent

Main functional group

ketone group attached to a phenyl ring

Usage

solvent in various industrial applications, production of pharmaceuticals, agrochemicals, and specialty chemicals

Health hazards

potential health hazards, should be handled with care and proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 111000-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,0 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111000-54:
(8*1)+(7*1)+(6*1)+(5*0)+(4*0)+(3*0)+(2*5)+(1*4)=35
35 % 10 = 5
So 111000-54-5 is a valid CAS Registry Number.

111000-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(4-phenylmethoxyphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 1-(4-Benzyloxy-phenyl)-2-chlor-propan-1-on

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:111000-54-5 SDS

111000-54-5Upstream product

111000-54-5Relevant articles and documents

PROCESS FOR PRODUCING OPTICALLY ACTIVE s-AMINO ALCOHOL

-

Page/Page column 30, (2008/06/13)

A process for easily producing an optically active β-amino alcohol useful as a pharmaceutical intermediate from an inexpensive, readily available starting material is provided. A readily available α-substituted ketone is reacted with an optically active amine to yield a diastereomer mixture of an optically active α-substituted aminoketone. One of the diastereomers is isolated optionally after the diastereomers are converted to salts with an acid. The optically active α-substituted aminoketone or a salt thereof thus isolated was stereoselectively reduced to yield an optically active β-substituted amino alcohol. The optically active β-substituted amino alcohol is subjected to hydrogenolysis to produce an optically active β-amino alcohol or a salt thereof.

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