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1,1-Dichlorohexan-2-one is a chemical compound with the molecular formula C6H10Cl2O. It is a colorless to pale yellow liquid with a pungent odor. This organic compound is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other chemicals. It is also known for its potential use as a solvent and a chemical building block in the synthesis of complex molecules. Due to its reactivity and the presence of two chlorine atoms, 1,1-dichlorohexan-2-one can undergo a range of chemical reactions, making it a versatile compound in the field of organic chemistry. However, it is important to handle this substance with care due to its potential toxicity and environmental impact.

2648-59-1

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2648-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2648-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2648-59:
(6*2)+(5*6)+(4*4)+(3*8)+(2*5)+(1*9)=101
101 % 10 = 1
So 2648-59-1 is a valid CAS Registry Number.

2648-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dichloro-2-hexanone

1.2 Other means of identification

Product number -
Other names 1,1-Dichlor-hexan-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:2648-59-1 SDS

2648-59-1Relevant academic research and scientific papers

Conversion of alkynes into α,α-dichloro ketones and α,α-dichlorodimethyl ketals using trichloroisocyanuric acid

Hiegel, Gene A.,Bayne, Christopher D.,Ridley, Brendt

, p. 1997 - 2002 (2003)

Trichloroisocyanuric acid reacts with alkynes in the presence of water in acetone or acetonitrile to form α,α-dichloro ketones and in methanol to form α,α-dichlorodimethyl ketals.

3-CYCLYL-5-(NITROGEN-CONTAINING 5-MEMBERED RING) METHYL-OXAZOLIDINONE DERIVATIVES AND THEIR USE AS ANTIBACTERIAL AGENTS

-

Page/Page column 59, (2008/06/13)

Compounds of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, (I) wherein -N-HET is, for example, (Ic) or (If) wherein R1 is (1-4C)alkyl;Q is selected from, for example, Q1 (Q1) wherein R2 and R

One-pot Synthesis of α,α-Dichloroketones from Alkynes Using the N,N-Dimethylformamide/HCl/Potassium Monoperoxysulfate System

Kim, Kye Kwang,Kim, Jae Nyoung,Kim, Kyoung Mahn,Kim, Hyoung Rae,Ryu, Eung K.

, p. 603 - 604 (2007/10/02)

The reaction of alkynes with N,N-dimethylformamide (DMF)/HCl/potassium monoperoxysulfate (Oxone, Aldrich) afforded the corresponding α,α-dichloroketones in good yields.

PRODUCTION OF 1,1,1-TRIHALOGENO-2-ALKANOLS AND SOME OF THEIR PROPERTIES

Bal'on, Ya. G.,Shul'man, M. D.,Vakulenko, L. I.

, p. 1231 - 1237 (2007/10/02)

The reaction of acyclic and carbocyclic carbonyl compounds with haloforms was studied in liquid ammonia and dimethylformamide in the presence of basic catalysts (t-BuOK, KOH).As a result of the reaction 1,1,1-trihalogeno-2-alkanols were obtained.They were used for the synthesis of 1,1,1-trihalogeno-2-methoxyalkanes, 1,1-dibromoalkenes, 1,1-dichloro-2-methoxyalkenes, and alkyl mono- and dichloromethyl ketones.

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