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Catalog Number:
33460
CAS Number:
1931895-14-5
N 3 -1,4- trans -CHC-OH
Purity:
≥ 99 % (dosage par titration, HPLC)
Synonym(s):
acide trans -4-azidocyclohexanecarboxylique
Antibiotic
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$68.90 /100 mg
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Product Information

N3-1,4-trans-CHC-OH, also known as 4-azidocyclohexane-1-carboxylic acid, is a versatile compound with significant potential in various fields, particularly in organic synthesis and medicinal chemistry. This compound features a unique azido group, which makes it an excellent candidate for click chemistry applications, allowing for the efficient formation of diverse chemical structures. Researchers can leverage its properties for the development of novel pharmaceuticals, as the azido functionality can facilitate the introduction of bioactive moieties into drug candidates.

In addition to its applications in drug development, N3-1,4-trans-CHC-OH can also be utilized in materials science for the synthesis of functionalized polymers and nanomaterials. Its ability to undergo selective reactions opens up possibilities for creating advanced materials with tailored properties. The compound's stability and reactivity make it a valuable tool for chemists looking to innovate in both academic and industrial settings, providing a pathway to explore new chemical entities and enhance existing formulations.

Synonyms
acide trans -4-azidocyclohexanecarboxylique
CAS Number
1931895-14-5
Purity
≥ 99 % (dosage par titration, HPLC)
Molecular Formula
C7H11N3O2
Molecular Weight
169.2
MDL Number
MFCD22989461
PubChem ID
23154170
Melting Point
70 - 72 °C
Appearance
Poudre cristalline blanche
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
acide trans -4-azidocyclohexanecarboxylique
CAS Number
1931895-14-5
Purity
≥ 99 % (dosage par titration, HPLC)
Molecular Formula
C7H11N3O2
Molecular Weight
169.2
MDL Number
MFCD22989461
PubChem ID
23154170
Melting Point
70 - 72 °C
Appearance
Poudre cristalline blanche
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Oui
DEA-regulated
Non
Warnings
-
Applications

N3-1,4-trans-CHC-OH is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of pharmaceutical agents, particularly in developing novel antibiotics and antiviral medications.
  • Bioconjugation: Its azide functional group allows for click chemistry applications, facilitating the attachment of biomolecules for targeted drug delivery systems.
  • Material Science: Used in creating advanced materials, it contributes to the development of polymers with enhanced properties, such as increased strength and thermal stability.
  • Diagnostics: The compound plays a role in the production of diagnostic agents, improving the specificity and sensitivity of imaging techniques in medical applications.
  • Research in Organic Chemistry: It is a valuable reagent for studying reaction mechanisms and developing new synthetic pathways, aiding chemists in exploring innovative chemical transformations.

Citations