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1587-29-7

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1587-29-7 Usage

Description

(E)-2,3-Dichloro-2-butene, with the molecular formula C4H6Cl2, is a colorless liquid characterized by a sharp, pungent odor. It is a chemical compound that serves as a versatile intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals. Additionally, it is utilized as a monomer in the production of polymers. Due to its highly flammable nature and potential hazards upon inhalation, ingestion, or skin contact, it is crucial to handle and store (E)-2,3-Dichloro-2-butene with caution and adhere to proper safety measures.

Uses

Used in Pharmaceutical Industry:
(E)-2,3-Dichloro-2-butene is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its role in this industry is crucial as it aids in the production of a range of medications that cater to different health needs.
Used in Agrochemical Industry:
In the agrochemical sector, (E)-2,3-Dichloro-2-butene is employed as an intermediate in the development of chemicals that are utilized in agriculture. These chemicals can include pesticides, herbicides, and other compounds that help in enhancing crop protection and yield.
Used in Polymer Production:
(E)-2,3-Dichloro-2-butene is also used as a monomer in the manufacturing process of polymers. Polymers are large molecules composed of repeating structural units, and this compound contributes to the formation of specific types of polymers that find applications in various industries, such as plastics, textiles, and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 1587-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1587-29:
(6*1)+(5*5)+(4*8)+(3*7)+(2*2)+(1*9)=97
97 % 10 = 7
So 1587-29-7 is a valid CAS Registry Number.

1587-29-7SDS

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 (E)-2,3-dichloro-2-butene

1.2 Other means of identification

Product number -
Other names 2,3-dichloro-but-2t-ene

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:1587-29-7 SDS

1587-29-7Relevant articles and documents

UNSATURATED COMPOUNDS. XV. LIQUID-PHASE LOW-TEMPERATURE CHLORINATION OF 2-CHLORO- AND 2,3-DICHLORO-2-BUTENES IN THE PRESENCE OF FERRIC CHLORIDE

Kaplanyan, E. E.,Mkrtchyan, A. M.,Voskanyan, E. S.

, p. 41 - 43 (2007/10/02)

The effect of anhydrous ferric chloride on the degree of normal and anomalous chlorination of 2-chloro- and 2,3-dichloro-2-butenes at low temperatures (-20 to 0 deg C) in the presence of tert-butyl pyrocatechol was investigated.It was established that the addition of ferric chloride leads to a significant decrease in the amount of anomalous chlorination products.At the same time an increase is observed in the chlorination rate of trans-2,3-dichloro-2-butene. During the chlorination of 2,3-dichloro-2-butene under the influence of ferric chloride the anomalous chlorination product 2,3,3-trichloro-1-butene isomerizes to 1,2,3-trichloro-2-butene.

INVESTIGATION IN THE FIELD OF UNSATURATED COMPOUNDS VI. LIQUID-PHASE CHLORINATION OF 2-HALOGENO-2-BUTENES

Mkryan, G. G.,Kaplanyan, E. E.,Mkryan, G. M.

, p. 1833 - 1836 (2007/10/02)

The liquid-phase chlorination of 2-halogeno-2-butenes in the presence of tert-butylpyrocatechol leads to the formation of the products from an anomalous reaction (2,3-dihalogeno-1-butenes), substitution of hydrogen at the double bond (2,3-dihalogeno-2-butenes), and normal addition (2,2,3-trihalogenobutanes).The ratios of these compounds are 70:6:24 in the case of 2-chloro-2-butene and 54:7.5:38.5 in the case of 2-bromo-2-butene.During the chlorination of 2-chloro-2-butene in the presence of sodium bicarbonate the formation of 3-chloro-2-butanol (20percent) was observed as a result of the combined addition of chlorine and water.

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