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Catalog Number:
29596
CAS Number:
1076197-05-1
Boc-4-(4-bromophenyl)-piperidine-4-carboxylic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
4-(4-Bromophenyl)-1-tert-butoxycarbonyl-piperidine-4-carboxylic acid
Documents
$93.14 /250MG
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Product Information

Boc-4-(4-bromophenyl)-piperidine-4-carboxylic acid is a versatile compound widely utilized in pharmaceutical research and development. This compound features a unique structure that includes a bromophenyl group, which enhances its reactivity and potential as a building block in the synthesis of various bioactive molecules. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, making it an ideal candidate for complex organic synthesis, particularly in the development of novel therapeutic agents. Researchers appreciate its stability and ease of handling, which facilitate efficient laboratory workflows.

In the pharmaceutical industry, Boc-4-(4-bromophenyl)-piperidine-4-carboxylic acid serves as a crucial intermediate in the synthesis of piperidine derivatives, which are known for their diverse biological activities, including analgesic and anti-inflammatory properties. Its application extends to medicinal chemistry, where it aids in the design of compounds targeting various diseases. The compound's unique properties and functional groups make it a valuable asset for researchers aiming to innovate and develop new therapeutic solutions.

Synonyms
4-(4-Bromophenyl)-1-tert-butoxycarbonyl-piperidine-4-carboxylic acid
CAS Number
1076197-05-1
Purity
≥ 99% (HPLC)
Molecular Formula
C17H22BrNO4
Molecular Weight
384.27
MDL Number
MFCD11226814
PubChem ID
45356721
Melting Point
184-190 ?C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
4-(4-Bromophenyl)-1-tert-butoxycarbonyl-piperidine-4-carboxylic acid
CAS Number
1076197-05-1
Purity
≥ 99% (HPLC)
Molecular Formula
C17H22BrNO4
Molecular Weight
384.27
MDL Number
MFCD11226814
PubChem ID
45356721
Melting Point
184-190 ?C
Appearance
White powder
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

Boc-4-(4-bromophenyl)-piperidine-4-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of analgesics and anti-inflammatory drugs. Its unique structure allows for modifications that enhance therapeutic efficacy.
  • Organic Synthesis: It is employed in organic synthesis as a building block for creating complex molecules. Researchers in academia and industry use it to streamline the synthesis of compounds with potential biological activity.
  • Drug Design: The compound's structural features make it valuable in drug design processes, particularly in creating targeted therapies for neurological disorders. Its ability to interact with specific receptors can lead to the development of more effective treatments.
  • Material Science: In material science, it is used to develop functionalized polymers and materials that exhibit desirable properties, such as improved thermal stability and mechanical strength, making it relevant in various industrial applications.
  • Research in Chemical Biology: This compound is utilized in chemical biology for probing biological systems, allowing researchers to study the effects of specific molecular interactions in cellular environments, which can lead to new insights in disease mechanisms.

Citations