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CAS 5417-17-4

2-Chloro-3,4-dimethoxybenzaldehyde TCI C1997

2-Chloro-3,4-dimethoxybenzaldehyde TCI C1997
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2-Chloro-3,4-dimethoxybenzaldehyde is a chemical compound widely used in the synthesis of complex organic molecules. As a building block in organic chemistry, it serves as a key intermediate in the development of compounds with specific biological activities. Its molecular structure features a benzene ring substituted with a chloro group and two methoxy groups, along with an aldehyde group at the 1-position. This unique structure allows it to participate in various chemical reactions, making it a versatile reagent in synthetic pathways.

The compound is valued for its stability under controlled conditions and its solubility in common organic solvents such as ethyl acetate and acetone. These properties facilitate efficient processing and purification in laboratory settings. Additionally, its chemical versatility enables it to be used in nucleophilic reactions, condensation, and substitution processes. The ability to undergo multiple reaction types enhances its utility in synthetic chemistry.

In Indonesian laboratories, 2-Chloro-3,4-dimethoxybenzaldehyde is frequently employed in organic synthesis research, particularly in pharmaceutical and medicinal chemistry applications. Its role in designing complex molecules makes it an essential component for researchers working on drug development and bioactive compound synthesis. The compound's predictable behavior and compatibility with standard laboratory techniques further support its widespread use in academic and industrial research settings.

  • Organic synthesis: This compound is ideal for creating complex molecules due to its reactive aldehyde group and substituent groups.
  • Pharmaceutical research: It is used in the development of bioactive compounds and drug candidates due to its structural versatility.
  • Nucleophilic reactions: The aldehyde functionality allows it to participate in nucleophilic addition and substitution reactions.
  • Condensation reactions: Its structure supports participation in condensation processes, aiding in the formation of new carbon-carbon bonds.
  • Molecular design: It serves as a building block for designing diverse organic molecules with specific functional groups.

Brand TCI
CAS number 5417-17-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid or liquid depending on the specific formulation
Storage Store in a cool, dry place away from direct sunlight and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. For optimal preservation, it should be kept in a well-ventilated area, away from incompatible substances such as strong oxidizing agents. Standard laboratory safety practices should be followed when handling, including the use of personal protective equipment. Proper labeling and storage conditions ensure the compound remains suitable for use in chemical synthesis and research applications.

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