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2-Pentanone, 4-(acetyloxy)-5,5,5-trichloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33673-55-1

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33673-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33673-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,7 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33673-55:
(7*3)+(6*3)+(5*6)+(4*7)+(3*3)+(2*5)+(1*5)=121
121 % 10 = 1
So 33673-55-1 is a valid CAS Registry Number.

33673-55-1SDS

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 1,1,1-trichloro-4-oxopentan-2-yl acetate

1.2 Other means of identification

Product number -
Other names 4-Acetoxy-5,5,5-trichlor-pentan-2-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:33673-55-1 SDS

33673-55-1Downstream Products

33673-55-1Relevant academic research and scientific papers

Lewis Acid Catalysis of Ene Addition of Chloral and Bromal to Olefins; Product Studies

Benner, Jill P.,Gill, G. Bryon,Parrott, Stephen J.,Wallace, Brian

, p. 291 - 313 (2007/10/02)

The addition of chloral and bromal to a variety of alkyl-substituted alkenes has been investigated.The effect of the reaction of varying the Lewis acid catalyst and the structure of substrate have been studied.Anhydrous AlCl3 was found to be most effective catalyst, and ene-type adducts were the major products in most cases.Side reactions were observed with the less reactive systems leading, variously, to the formation of trihalogenoketones, hydrohalogenated ene adducts, and cyclic ethers.Conditions for optimising the yield of ene adducts were established in some cases.The trihalogenoketone by-products can be conveniently removed by a Grignard-type reaction.

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