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Catalog Number:
26761
CAS Number:
22809-37-6
6-Bromohexanoyl chloride
Purity:
≥ 98% (GC)
Documents
$18.53 /1G
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Product Information

6-Bromohexanoyl chloride is a versatile chemical compound widely utilized in organic synthesis and various industrial applications. This acyl chloride is known for its reactivity, making it an essential intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique bromine substituent enhances its electrophilic character, allowing for efficient acylation reactions. Researchers and industry professionals often leverage 6-Bromohexanoyl chloride in the synthesis of complex molecules, including the development of novel drug candidates and the modification of polymer materials.

The compound's ability to facilitate the introduction of hexanoyl groups into target molecules makes it particularly valuable in the creation of bioactive compounds. Its applications extend to the production of surfactants and other functional materials, where its reactivity can be harnessed to achieve desired properties. With its favorable characteristics, 6-Bromohexanoyl chloride stands out as a crucial building block for innovative chemical processes and product development.

CAS Number
22809-37-6
Purity
≥ 98% (GC)
Molecular Formula
C6H10BrClO
Molecular Weight
213.5
MDL Number
MFCD00000761
PubChem ID
89848
Appearance
Colorless to light yellow liquid
Conditions
Store at 0-8 °C
General Information
CAS Number
22809-37-6
Purity
≥ 98% (GC)
Molecular Formula
C6H10BrClO
Molecular Weight
213.5
MDL Number
MFCD00000761
PubChem ID
89848
Appearance
Colorless to light yellow liquid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Bromohexanoyl chloride is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the production of various pharmaceutical agents, enabling the development of new medications with improved efficacy.
  • Organic Synthesis: It is commonly used in organic chemistry for acylation reactions, allowing chemists to modify existing compounds and create new derivatives with desired properties.
  • Polymer Chemistry: The chemical plays a role in the synthesis of specialty polymers, which can be tailored for specific applications such as coatings, adhesives, and sealants.
  • Research and Development: Researchers utilize this compound in laboratory settings to explore reaction mechanisms and develop new synthetic pathways, contributing to advancements in chemical knowledge.
  • Bioconjugation: It is employed in bioconjugation processes to attach biomolecules to surfaces or other compounds, enhancing the functionality of diagnostic tools and therapeutic agents.

Citations