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2-Hexanone, 1,4-dichloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77958-30-6

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77958-30-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77958-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,5 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77958-30:
(7*7)+(6*7)+(5*9)+(4*5)+(3*8)+(2*3)+(1*0)=186
186 % 10 = 6
So 77958-30-6 is a valid CAS Registry Number.

77958-30-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dichloro-2-hexanone

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:77958-30-6 SDS

77958-30-6Downstream Products

77958-30-6Relevant academic research and scientific papers

Reactions of 2-(2-propenyl)-3-chloromethyloxirane with benzene

Akhmedov, M.A.,Sardarov, I.K.,Akhmedov, I.M.,Kostikov, R.R.,Babaev, N.M.,Shukyurova, M.B.

, p. 2025 - 2028 (2007/10/02)

The reaction of 2-(2-propenyl)-3-chloromethyloxirane with benzene in the presence of aluminum chloride gives a 3:6:1 mixture of 1,4-dichloro-2-hexanone, 1-chloro-4-phenyl-2-hexanone, and 1-chloro-3,4-diphenyl-2-hexanone

Acylation du (cyclopropylmethyl)trimethylsilane. Une nouvelle voie d'acces aux enones non conjuguees

Grignon-Dubois, M.,Dunogues, J.,Calas, R.

, p. 802 - 806 (2007/10/02)

Acylation of (cyclopropylmethyl)trimethylsilane using RCOCl/AlCl3 (R: saturated hydrocarbon group) constitutes a mild, convenient route to β,γ-unsaturated ketones free from the conjugated isomers.With α,β-unsaturated acyl chlorides a competitive reaction between the C-H and C-Si allylic cleavage is observed whereas chloroacetyl chloride affords the γ,δ-ethylenic corresponding ketone.A mechanism involving the catalytic role of HCl in the formation of β,γ-unsaturated and chloroketones is proposed.

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