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6611-78-5

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6611-78-5 Usage

General Description

4-DICHLOROMETHYL-4-METHYL-2,5-CYCLOHEXADIENONE is a chemical compound with the molecular formula C8H8Cl2O. It is a yellow to brown liquid with a pungent odor, and is primarily used as an intermediate in the manufacture of pharmaceuticals and agrochemicals. 4-DICHLOROMETHYL-4-METHYL-2,5-CYCLOHEXADIENONE is known to be a potent irritant to the eyes, skin, and respiratory system, and can cause irritation upon contact. It is also considered to be a hazardous substance and should be handled with care. This chemical is not widely used or encountered in everyday life, but it is important to be aware of its potential hazards and take necessary precautions when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 6611-78-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6611-78:
(6*6)+(5*6)+(4*1)+(3*1)+(2*7)+(1*8)=95
95 % 10 = 5
So 6611-78-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Cl2O/c1-8(7(9)10)4-2-6(11)3-5-8/h2-5,7H,1H3

6611-78-5SDS

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 4-(dichloromethyl)-4-methylcyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 4-Dichlormethyl-4-methyl-cyclohexa-2,5-dienon

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:6611-78-5 SDS

6611-78-5Relevant articles and documents

Miller

, p. 751 (1969)

Electrochemical reduction of 4-methyl-4-(trichloromethyl)cyclohexa-2,5- dien-1-one

Moiseeva,Gavrilova,Vykhodtseva,Nikolaeva,Krut'Ko,Beloglazkina

, p. 1074 - 1078 (2014)

The properties of 4-methyl-4-(trichloromethyl)cyclohexa-2,5-dien-1-one which contains the trichloromethyl substituent at a quaternary carbon atom have been studied by cyclic voltammetry, rotating disk electrode voltammetry, and preparative electrolysis. Reductive dehalogenation involves initial two-electron reductive elimination of one of the geminal chlorine atoms followed by consecutive addition of proton, simultaneous elimination of the two residual halogen atoms to form carbene, and rearrangement of cyclohexadienone into the corresponding 4-methylcyclohepta-2,4,6-trien-1-one.

POSSIBILITY OF THE FORMATION OF CHLOROSUBSTITUTED TROPONE RINGS UNDER ZINCKE-SUHL REACTION CONDITIONS

Sergeev, S. V.,Nikanorov, V. A.,Rosenberg, V. I.,Reutov, O. A.

, p. 790 - 792 (2007/10/02)

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