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Catalog Number:
23183
CAS Number:
21436-03-3
(1 S ,2 S )-(+)-1,2-diaminocyclohexane
Purity:
≥ 99 % (dosage)
Hazmat
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Product Information

(1S,2S)-(+)-1,2-Diaminocyclohexane is a versatile chiral diamine that plays a crucial role in various chemical synthesis processes. Known for its unique stereochemistry, this compound is widely utilized in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to act as a chiral building block makes it particularly valuable in asymmetric synthesis, allowing researchers to create enantiomerically pure compounds that are essential in drug development. Additionally, it serves as a ligand in coordination chemistry, enhancing the efficacy of catalysts in various reactions.

The compound's stability and reactivity make it an excellent choice for applications in organic synthesis, particularly in the preparation of amino acids and other biologically active molecules. Its use in the development of chiral catalysts has opened new avenues in green chemistry, promoting more sustainable practices in chemical manufacturing. With its broad applicability and significant advantages over non-chiral counterparts, (1S,2S)-(+)-1,2-Diaminocyclohexane is an indispensable tool for researchers and industry professionals aiming to innovate and improve their chemical processes.

CAS Number
21436-03-3
Purity
≥ 99 % (dosage)
Molecular Formula
C6H14N2
Molecular Weight
114.2
MDL Number
MFCD00062986
PubChem ID
4610
Melting Point
40 - 43 ?C
Appearance
Solide blanc
Boiling Point
104 - 110 ?C
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
21436-03-3
Purity
≥ 99 % (dosage)
Molecular Formula
C6H14N2
Molecular Weight
114.2
MDL Number
MFCD00062986
PubChem ID
4610
Melting Point
40 - 43 ?C
Appearance
Solide blanc
Boiling Point
104 - 110 ?C
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(1S,2S)-(+)-1,2-Diaminocyclohexane is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a chiral building block in the synthesis of various pharmaceuticals, enhancing the efficacy and reducing side effects of medications.
  • Catalysis: It acts as a ligand in asymmetric catalysis, improving reaction selectivity and yield in the production of fine chemicals and agrochemicals.
  • Material Science: Used in the development of polymers and resins, it contributes to creating materials with enhanced mechanical properties and thermal stability.
  • Biochemistry: This compound is valuable in studying enzyme interactions and protein folding, aiding researchers in understanding biological processes at a molecular level.
  • Environmental Applications: It can be used in the formulation of biodegradable chelating agents, promoting greener chemistry practices in various industries.

Citations