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TCI

CAS 5162-82-3

3-Chloro-4-methylbenzoic Acid TCI C2462

3-Chloro-4-methylbenzoic Acid TCI C2462

Chemical Identity

Other names
3-Chloro-p-toluic Acid
CAS No.
5162-82-3
PubChem
CID 78840·SID 125307678
Formula
C8H7ClO2
Molecular weight
170.59 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
3-chloro-4-methylbenzoic acid
SMILES
CC1=C(C=C(C=C1)C(=O)O)Cl
InChIKey
SDKUOEOJAXGCLU-UHFFFAOYSA-N
MDL
MDL00045841
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3-Chloro-4-methylbenzoic Acid is a versatile chemical compound widely used in laboratory settings for its reactivity and structural versatility. It belongs to the class of non-heterocyclic building blocks and is commonly employed in organic synthesis. This compound serves as a key intermediate in the development of aromatic compounds and their derivatives, making it essential for researchers working in synthetic chemistry. Its presence in various chemical reactions allows for the creation of more complex molecules, supporting a wide range of experimental applications.

The compound's stability and controlled reactivity make it a preferred choice in laboratory environments. Its predictable melting point and solubility characteristics facilitate efficient isolation and purification processes. Additionally, its resistance to degradation under standard laboratory conditions ensures reliable results over time. These properties contribute to its widespread use in both academic and industrial research settings.

In Indonesian laboratories, 3-Chloro-4-methylbenzoic Acid is frequently utilized in organic chemistry research. It is commonly found in academic institutions and research centers, where it supports the synthesis of various organic compounds. Its availability and reliability make it a staple in chemical laboratories across Indonesia, contributing to the advancement of scientific studies and educational programs.

  • Organic synthesis: This compound is ideal for creating aromatic derivatives due to its reactive carboxylic acid group and chloro and methyl substituents.
  • Esterification reactions: The carboxylic acid functionality allows for the formation of esters, a common reaction in synthetic chemistry.
  • Substitution reactions: Its aromatic ring structure makes it suitable for electrophilic substitution processes in laboratory settings.
  • Research and development: It is frequently used in R&D projects to develop new compounds and materials.
  • Educational experiments: Its stability and predictable behavior make it a valuable teaching tool in undergraduate and graduate chemistry courses.

Brand TCI
CAS number 5162-82-3
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid
Storage Store in a cool, dry place away from direct light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. It is important to ensure proper ventilation when working with this material to avoid inhalation of vapors. Storage conditions should be consistent to maintain its chemical stability and ensure safe handling in laboratory environments.

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