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1,2,3-trichloro-2-(chloromethyl)propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18963-00-3

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18963-00-3 Usage

Physical state

Colorless liquid

Odor

Strong, chloroform-like

Usage

Intermediate in the synthesis of other organic compounds

Hazardous nature

Yes

Potential health effects

Skin and eye irritation, respiratory and central nervous system effects

Precaution

Handle and store with caution

Exposure risk

High levels can be harmful to human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 18963-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,6 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18963-00:
(7*1)+(6*8)+(5*9)+(4*6)+(3*3)+(2*0)+(1*0)=133
133 % 10 = 3
So 18963-00-3 is a valid CAS Registry Number.

18963-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-trichloro-2-(chloromethyl)propane

1.2 Other means of identification

Product number -
Other names 1.2.3.21-Tetrachlor-2-methyl-propan

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:18963-00-3 SDS

18963-00-3Downstream Products

18963-00-3Relevant academic research and scientific papers

Generation of radical species in surface reactions of chlorohydrocarbons and chlorocarbons with fluorinated gallium(III) oxide or indium(III) oxide

Thomson

, p. 1881 - 1885 (2007/10/03)

The reactions of C1 and C2 chlorohydrocarbons and chlorocarbons have been studied with the Lewis acid catalysts fluorinated gallium(III) oxide and fluorinated indium(III) oxide, respectively. Product analysis shows chlorine-for-fluorine exchange reactions together with the formation of 2-methylpropane and its chlorinated analogues 2-chloromethyl-1,3-dichloropropane and 2-chloromethyl-1,2,3-trichloropropane. Reactivities of the chlorohydrocarbon probe molecules show fluorinated gallium(III) oxide to be a stronger Lewis acid than fluorinated indium(III) oxide. The formation of the symmetrical butyl compounds is consistent with the generation of surface radical species and is also consistent with a 1,2-migration mechanism operating within radical moieties at the Lewis acid surface.

Synthesis and Characterization of Polychlorinated Isobutenes

Schulze, K.,Hartmann, S.,Krueger, H.,Muehlstaedt, M.,Richter, C.,Richter, H.

, p. 433 - 442 (2007/10/02)

The preparation of polychlorinated methallylic chlorides by continuous chlorination of isobutene with different ratios of chlorine and following HCl-elimination is described.The structure is proved by reaction of the polychlorinated isobutenes with sodium thiolacetate and potassium thiocyanate and by spectroscopic methods.

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