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74316-25-9

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74316-25-9 Usage

Type

Organic compound

Consists of

Ketone group and chlorophenol group

Usage

Solvent in various industrial processes, precursor in the production of pharmaceuticals and fragrances, synthesis of other organic compounds, and flavoring agent in the food industry

Safety precautions

Can be irritating to the skin and eyes, may cause respiratory issues if inhaled in large amounts, important to use proper safety equipment and procedures when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 74316-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,1 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74316-25:
(7*7)+(6*4)+(5*3)+(4*1)+(3*6)+(2*2)+(1*5)=119
119 % 10 = 9
So 74316-25-9 is a valid CAS Registry Number.

74316-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(2-hydroxyphenyl)propan-1-one

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:74316-25-9 SDS

74316-25-9Downstream Products

74316-25-9Relevant articles and documents

A REEXAMINATION OF THE RETRO-FRIES REARRANGEMENT OF SOME o-HYDROXYKETONES

Martin, Robert,Lafrance, Jean Ronald,Demerseman, Pierre

, p. 539 - 548 (2007/10/02)

The retro-Fries rearrangement, catalyzed by protic and Lewis acids, was studied for some o-hydroxyketones.The results are consistent with the mechanism of an heterolytic cleavage and rearrangement.It appears that, in general, Lewis acids do not induce the retro-Fries rearrangement of o-hydroxyketones.However, in certain cases, it may be brought about the presence of a protic acid generated in situ, from a solvent-catalyst interaction.

A model for a molecular mechanism of anticoagulant activity of 3-substituted 4-hydroxycoumarins

Silverman

, p. 5421 - 5423 (2007/10/02)

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