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Alpha Bromo 2 Chlorophenylacetic Acid

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Alpha Bromo 2 Chlorophenylacetic Acid Specification

HS Code
Not available

Refractive Rate
Not available

Structural Formula
C8H6BrClO2

Molecular Weight
249.49 g/mol

Molecular Formula
C8H6BrClO2

Boiling point
Not available

Smell
Odorless

Classification
Organic Acid

Organic Acid Types
Carboxylic Acid

Grade
Industrial Grade

Purity
Not available

Application
Used as an intermediate in organic synthesis

Appearance
White crystalline powder

CAS No
29541-51-1

EINECS No
Not available

Other Names
Alpha-Bromo-2-Chlorophenylacetic Acid

Usage
Chemical synthesis and research purposes

Melting Point
116-118C

Density
Gram per cubic centimeter(g/cm3)

Solubility
Slightly soluble in water

Raw Material
Relevant organic precursors

About Alpha Bromo 2 Chlorophenylacetic Acid

With the help of our qualified experts, we are able to offer an extensive variety of Alpha-Bromo-2-Chlorophenylacetic Acid that is high on demand in the pharmaceutical and molecular formula is C8H6BrClO2. Alpha bromo-2-chlorophenylacetic acid is used as an intermediate in the preparation of biologically active compounds, for example, the antithrombotic Clopidogrel (C587250). They are appropriately tried on different parameters before they are supplied in the market.

Features:

White to off-white solid appearance
Melting Point: 107 C to 112 C
Purity By HPLC: N.L.T 99.0 %
Moisture by KFR: N.M.T. 0.5 %

Key Characteristics

Alpha Bromo 2 Chlorophenylacetic Acid stands out due to its stable white crystalline appearance, high purity, and industrial-grade quality. Its slightly water-soluble, odorless nature ensures ease of handling in laboratory and manufacturing environments. Widely recognized under the chemical classification of carboxylic acids, it offers versatility for multiple synthesis routes.

Applications and Uses

This compound primarily serves as an intermediate in organic synthesis, facilitating complex chemical reactions. Its use spans chemical research and industrial manufacturing where efficient synthesis of target molecules is needed. Because of its specificity, it is essential in laboratories and in developing new organic compounds.

FAQs of Alpha Bromo 2 Chlorophenylacetic Acid:

Q: How is Alpha Bromo 2 Chlorophenylacetic Acid typically used in the chemical industry?

A: Alpha Bromo 2 Chlorophenylacetic Acid is mainly used as an intermediate in the synthesis of more complex organic compounds, making it valuable for chemical research and industrial manufacturing processes.

Q: What is the benefit of using Alpha Bromo 2 Chlorophenylacetic Acid as an intermediate?

A: Using this compound as an intermediate enables the efficient synthesis of diverse chemical entities. Its reactive carboxylic acid group facilitates various organic transformations, streamlining the production of pharmaceuticals and specialty chemicals.

Q: When should Alpha Bromo 2 Chlorophenylacetic Acid be handled with special care?

A: Special care should be taken during handling in synthesis or manufacturing environments, as with all chemical reagents. Appropriate personal protective equipment and safety measures are recommended to avoid exposure despite the compound being odorless and of relatively stable appearance.

Q: What are the main raw materials for producing Alpha Bromo 2 Chlorophenylacetic Acid?

A: The principal raw materials are relevant organic precursors, generally aromatic compounds that provide the necessary phenyl, bromine, and chlorinated components required for the synthesis.

Q: Where is Alpha Bromo 2 Chlorophenylacetic Acid most commonly sourced from?

A: This compound is most commonly sourced from industrial manufacturers, exporters, and suppliers in India, known for providing high-grade speciality chemicals for global markets.

Q: What is the process for applying Alpha Bromo 2 Chlorophenylacetic Acid in laboratory research?

A: In laboratory research, it is typically introduced as an intermediate reagent in stepwise organic synthesis, participating in transformations to yield structurally advanced target molecules.

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