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2431-50-7

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2431-50-7 Usage

Safety Profile

Confirmed carcinogen. Poison by ingestion. When heated to decomposition it emits toxic fumes of Cl-.

Check Digit Verification of cas no

The CAS Registry Mumber 2431-50-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2431-50:
(6*2)+(5*4)+(4*3)+(3*1)+(2*5)+(1*0)=57
57 % 10 = 7
So 2431-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H5Cl3/c1-3(6)4(7)2-5/h4H,1-2H2

2431-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4-Trichloro-1-butene

1.2 Other means of identification

Product number -
Other names 2,3,4-trichloro-1-naphthol

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:2431-50-7 SDS

2431-50-7Relevant articles and documents

Transmetallation of β-allenyl silanes: Efficient synthesis of dienyl chlorostannanes and chlorostibines

Lahrech, Mokhtar,Thibonnet, Jerome,Hacini, Salih,Santelli, Maurice,Parrain, Jean-Luc

, p. 644 - 645 (2002)

The reaction of 1-trimethylsilylbuta-2,3-diene with tin tetrachloride, antimony trichloride or antimony pentachloride gave the corresponding buta-1,3-dien-2-yl halostannane or stibine derivatives; this ligand exchange was extended to other β-allenylsilane

Chlorination of chloroolefins C3-C4

Levanova,Strizhakova,Sokolov,Aseev,Lapidus

, p. 255 - 257 (2007/10/03)

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CHEMISTRY OF DIENES AND THEIR DERIVATIVES. XVII. LOW-TEMPERATURE CHLORINATION OF 2-CHLORO- AND 1,2-DICHLORO-1,3-BUTADIENES IN THE PRESENCE OF AN INHIBITOR OF RADICAL REACTIONS

Mkryan, G. M.,Airapetyan, R. Kh.,Mkryan, G. G.,Kaplanyan, E. E.

, p. 1242 - 1247 (2007/10/02)

During the chlorination of chloroprene (80-85percent conversion) in carbon tetrachloride at -5 to 0 deg C in the presence of tert-butylpyrocatechol 1,2-dichloro-1,3-butadiene, 3,3,4-trichloro-1-butene, 2,3,4-trichloro-1-butene, and 1,2,4-trichloro-2-butene are formed in percentage ratios of 20.4:6.7:3.4:69.5.During chlorination to total conversion of chloroprene under these conditions a series of other compounds are also formed as a result of the further chlorination of 1,2-dichloro-1,3-butadiene and 3,3,4-trichloro-1-butene.During the chlorination of 1,2-dichloro-1,3-butadiene to a high degree of conversion 1,2,4-trichloro-1,3-butadiene, 1,2,3,4-tetrachloro-1-butene, and 1,1,2,4-tetrachloro-2-butene are formed in ratios of 11.4:49:39.6.

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