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2-Bromoethyl chloroacetate is an organic compound with the chemical formula C4H6BrClO2. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 191.45 g/mol. 2-bromoethyl chloroacetate is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is produced through the reaction of 2-bromoethanol with chloroacetic acid in the presence of a catalyst. Due to its reactivity, 2-bromoethyl chloroacetate is often used in the preparation of alkylating agents and as a building block for more complex molecules. It is important to handle 2-bromoethyl chloroacetate with care, as it can be harmful if inhaled, ingested, or absorbed through the skin, and it may cause irritation to the eyes, skin, and respiratory system.

5406-22-4

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5406-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5406-22-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5406-22:
(6*5)+(5*4)+(4*0)+(3*6)+(2*2)+(1*2)=74
74 % 10 = 4
So 5406-22-4 is a valid CAS Registry Number.

5406-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Chlor-essigsaeure-(2-brom-4-methyl-anilid)

1.2 Other means of identification

Product number -
Other names chloro-acetic acid-(2-bromo-ethyl ester)

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:5406-22-4 SDS

5406-22-4Downstream Products

5406-22-4Relevant academic research and scientific papers

Reactions of 1,3-Dioxacyclanes with Acid Halides. A New Synthesis for ω-Halohydrine Esters

Kwiatkowski, Stefan,Wolinski, Andrzej

, p. 869 - 872 (2007/10/02)

Reaction of 1,3-dioxolanes and 1,3-dioxanes with aliphatic acid chlorides and bromides yields 2- or 3-halohydrine esters. - Keywords: 1,3-Dioxolanes and 1,3-dioxanes, ring opening of

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