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

66241-39-2

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66241-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66241-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,4 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66241-39:
(7*6)+(6*6)+(5*2)+(4*4)+(3*1)+(2*3)+(1*9)=122
122 % 10 = 2
So 66241-39-2 is a valid CAS Registry Number.

66241-39-2SDS

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-chlorooctan-3-one

1.2 Other means of identification

Product number -
Other names 2-chloro-octan-3-one

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:66241-39-2 SDS

66241-39-2Relevant academic research and scientific papers

Iridium-catalyzed 1,3-hydrogen shift/chlorination of allylic alcohols

Ahlsten, Nanna,Gomez, Antonio Bermejo,Martin-Matute, Belen

supporting information, p. 6273 - 6276 (2013/07/05)

Tandem: Allylic alcohols react with N-chlorosuccinimide (NCS) in a tandem 1,3-H shift/C-Cl bond formation leading to α-chloroketones and α-chloroaldehydes. The reactions proceed with complete selectivity to give single constitutional isomers of monochlorinated carbonyl compounds. The utility of the transformation is illustrated by the straightforward synthesis of 4,5-disubstituted 2-aminothiazoles from allylic alcohols. Copyright

Mild and efficient α-chlorination of carbonyl compounds using ammonium chloride and oxone (2KHSO5·KHSO4· K2SO4)

Swamy, Peraka,Kumar, MacHarla Arun,Reddy, Marri Mahender,Narender, Nama

supporting information; experimental part, p. 432 - 434 (2012/06/01)

A simple protocol for the α-monochlorination of ketones and 1,3-dicarbonyl compounds utilizing NH4Cl as a source of chlorine and Oxone as an oxidant in methanol without catalyst is presented. The reaction proceeds at ambient temperature in yields ranging from moderate to excellent.

OXIDATION OF OLEFINS USING CHROMIC ANHYDRIDE-CHLOROTRIMETHYLSILANE. A CONVENIENT SYNTHESIS OF α-CHLORO KETONES.

Lee, Jong Gun,Ha, Dong Soo

, p. 193 - 196 (2007/10/02)

Disubstituted internal olefins are oxidized selectively to α-chloro ketones in excellent yields from the reaction with chromic anhydride-chlorotrimethylsilane in carbon tetrachloride.

Metal-Catalyzed Organic Photoreactions. One-Step Synthesis of Chlorinated Ketones from Olefins by Photooxidation in the Presence of Iron(III) Chloride

Kohda, Akira,Ueda, Keiko,,Sato, Tadashi

, p. 509 - 515 (2007/10/02)

Under photooxidation in pyridine in the presence of FeCl3, mono- and disubstituted olefins gave α-chloro ketones, while tri- and tetrasubstituted olefins gave dichloro ketones with a C-C bond cleavage.The reaction was interpreted in terms of an electron-transfer mechanism occurring within the coordination sphere of the iron ion

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