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1-Bromo-2-chloroethene, also known as 1,2-dichloro-1-bromoethene or 1,2-dichloro-1-bromoethylene, is a halogenated hydrocarbon with the chemical formula C2H2BrCl. It is a colorless liquid with a pungent odor and is used as an industrial chemical, particularly in the production of pharmaceuticals and agrochemicals. Due to its reactivity and potential health risks, it is important to handle 1-bromo-2-chloroethene with caution, as it can cause irritation to the eyes, skin, and respiratory system, and may have long-term effects on the liver and kidneys.

3018-09-5

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3018-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3018-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,1 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3018-09:
(6*3)+(5*0)+(4*1)+(3*8)+(2*0)+(1*9)=55
55 % 10 = 5
So 3018-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C2H2BrCl/c3-1-2-4/h1-2H/b2-1+

3018-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-chloro-Ethene

1.2 Other means of identification

Product number -
Other names Ethene, 1-bromo-2-chloro-

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:3018-09-5 SDS

3018-09-5Downstream Products

3018-09-5Relevant academic research and scientific papers

Dynamics of endoergic substitution reactions. II. Br + -> Cl +

Robinson, Gary N.,Continetti, Robert E.,Lee, Yuan T.

, p. 6238 - 6246 (2007/10/02)

We have extended the crossed beams studies described in the preceding paper to the reactions of Br atoms with 1,1- and trans-dichloroethylene.The shapes of the product translational energy distributions and excitation functions for both reactions support our previous conclusion that Cl elimination from Br-R-Cl collision complexes can compete with Br elimination only in the limit that few vibrational modes of the complex are active in energy redistribution.The substitution cross section for the Br + CH2CCl2 reaction is considerably lower than that for the Br + trans-CHClCHCl reaction in the collision energy range 15-25 kcal/mol, suggesting that steric effects play a dominant role in determining the relative magnitudes of the cross sections.

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