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1,2,3,4-tetrachlorocyclopentane is a chemical compound characterized by a five-membered ring structure with four chlorine atoms attached. It is a colorless liquid at room temperature, exhibiting limited solubility in water but good solubility in various organic solvents. Recognized for its utility in organic synthesis, 1,2,3,4-tetrachlorocyclopentane also presents environmental and health concerns due to its potential toxicity and harmful effects on aquatic life.

1122-14-1

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1122-14-1 Usage

Uses

Used in Organic Synthesis:
1,2,3,4-tetrachlorocyclopentane is utilized as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of desired organic compounds.
Used in Chemical Research:
In the field of chemical research, 1,2,3,4-tetrachlorocyclopentane serves as a subject of study to understand its properties, reactivity, and potential applications, as well as to explore methods for safe handling and disposal to mitigate its environmental impact.
Used in Industrial Applications:
While specific industrial applications are not detailed in the provided materials, 1,2,3,4-tetrachlorocyclopentane may be employed in certain industrial processes that require its unique chemical properties, always with consideration for the necessary safety precautions due to its harmful nature.

Check Digit Verification of cas no

The CAS Registry Mumber 1122-14-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1122-14:
(6*1)+(5*1)+(4*2)+(3*2)+(2*1)+(1*4)=31
31 % 10 = 1
So 1122-14-1 is a valid CAS Registry Number.

1122-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrachloro-cyclopentane

1.2 Other means of identification

Product number -
Other names 1,2,3,4-Tetrachlor-cyclopentan

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:1122-14-1 SDS

1122-14-1Relevant academic research and scientific papers

Manufacturing method of 1,2-dichlorohexafluorocyclopentene

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Paragraph 0042, (2019/05/15)

Disclosed is a manufacturing method of 1,2-dichlorohexafluorocyclopentene. The first reaction uses dicyclopentadiene as a starting material and nitrogen gas or another inert gas as a diluting agent in a gas-phase thermal cracking reaction to obtain cyclopentadiene. The second reaction uses cyclopentadiene as a starting material in a liquid phase chlorination reaction with chlorine gas to obtain 1,2,3,4-tetrachlorocyclopentane. The third reaction uses 1,2,3,4-tetrachlorocyclopentane as a starting material in a gas-phase chlorination and fluorination reaction with hydrogen fluoride and chlorine gas in the presence of a chromium-based catalyst to obtain 1,2-dichlorohexafluorocyclopentene. The method uses easily acquired starting material and a stable fluorination catalyst, provides a high yield for a target product, and is applicable for large-scale continuous gas-phase production of 1,2-dichlorohexafluorocyclopentene.

Industrial production method for perfluorocyclopentene

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Paragraph 0032; 0033; 0035; 0036; 0037; 0038, (2018/07/07)

The invention discloses an industrial production method for perfluorocyclopentene, and belongs to the field of fine chemical intermediate synthesis. Cyclopentene, chlorine and pyridine hydrofluoride which are used as raw materials undergo high-temperature chlorination in a solvent sulfolane to obtain octachlorocyclopentene, and the octachlorocyclopentene and pyridine hydrofluoride undergo high-temperature fluorination substitution to obtain the perfluorocyclopentene. Residues obtained after the separation of the product undergo reduced pressure distillation to obtain the solvent sulfolane which can be reused. The method allows the product yield to reach 45-55%, the product content to be more than 99%, the water content to be less than 0.1% and the chloride ion content to be less than 0.1%. The method has the advantages of no pollution in the production process, green production process, high yield, simple steps, facilitation of the reduction of the production cost, high product purity, and facilitation of later application.

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