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2,2-dichloro-3,3,4,4-tetramethylcyclobutanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66239-90-5

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66239-90-5 Usage

Family

Cyclobutanones

Reactivity

Highly reactive

Flammability

Flammable liquid

Usage

Starting material in organic synthesis, reagent in chemical reactions, intermediate in production of pharmaceuticals, agrochemicals, and other fine chemicals

Toxicity

Mild to moderate acute toxicity

Handling

Should be handled with care in a controlled environment

Check Digit Verification of cas no

The CAS Registry Mumber 66239-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,3 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66239-90:
(7*6)+(6*6)+(5*2)+(4*3)+(3*9)+(2*9)+(1*0)=145
145 % 10 = 5
So 66239-90-5 is a valid CAS Registry Number.

66239-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dichloro-3,3,4,4-tetramethylcyclobutan-1-one

1.2 Other means of identification

Product number -
Other names dichloro-2,2-tetramethyl-3,3,4,4 cyclobutanone

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:66239-90-5 SDS

66239-90-5Relevant academic research and scientific papers

Titanium(IV) chloride-mediated ring cleavage and Michael addition of 3,3-dialkylcyclobutanones and 3-[(trimethylsilyl)methyl]-cyclobutanones

Okuno, Ryosuke,Matsuo, Jun-Ichi,Ishibashi, Hiroyuki

experimental part, p. 793 - 797 (2012/08/07)

β′-Chloro and β′,γ′-unsaturated trichlorotitanium enolates, which were formed in situ by titanium(IV) chloride-mediated ring cleavage of 3,3-dialkylcyclobutanones and 3-[(trimethylsilyl)methyl]cyclobutanones, reacted with enones to give Michael adducts wi

Facile activation of zinc. Preparation of cyclobutanones via dichloroketene and cyclopropanes using the Simmons-Smith reaction

Stenstrom

, p. 2801 - 2810 (2007/10/02)

Zinc powder activated by heating in an inert atmosphere gave good yields when used for the title reactions. The very easy work up procedure for the cyclobutanones further increases the potential of the method.

Selective synthesis of glutaric acids from olefins

Depres,Greene

, p. 7065 - 7068 (2007/10/02)

Six representative glutaric acids have been regio- and stereoselectively prepared from the corresponding olefins in 49 to 65% overall yields. α,α-Dichlorocyclopentanones, readily available from the olefins by three-carbon annelation, are transformed via chloro enol acetates to the glutaric acids.

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