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CAS 365996-30-1

(1S,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine TCI B3483

(1S,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine TCI B3483

Chemical Identity

CAS No.
365996-30-1
PubChem
CID 1514389·SID 135727094
Formula
C11H22N2O2
Molecular weight
214.30 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl N-[(1S,2R)-2-aminocyclohexyl]carbamate
SMILES
CC(C)(C)OC(=O)N[C@H]1CCCC[C@H]1N
InChIKey
AKVIZYGPJIWKOS-BDAKNGLRSA-N
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(1S,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine is a chiral building block widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in organic chemistry research, particularly in the development of chiral compounds with applications in pharmacology and biochemistry. Its complex structure allows for highly specific chemical reactions, such as deprotonation and substitution, making it a valuable tool for researchers aiming to design molecules with targeted interactions with enzymes or receptors.

The compound's tert-butoxycarbonyl (Boc) group provides stability under certain conditions and facilitates the conversion to its active form through Boc cleavage. This property makes it ideal for applications requiring precise control over molecular structure and function. Its versatility in synthetic pathways and compatibility with various reaction conditions further enhance its appeal in both academic and industrial research settings.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in pharmacology and the synthesis of chiral compounds. It is frequently employed by research institutions and universities to develop new drugs and understand molecular interactions. Its role in creating molecules with specific biological activities underscores its importance in advancing scientific research in the region.

TCI brochures (PDF)

  • Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the creation of enantiomerically pure compounds with specific biological activities.
  • Chiral Compound Development: Its use in chiral compound development allows researchers to design molecules with targeted interactions with enzymes or receptors, enhancing drug efficacy.
  • Organic Chemistry Research: The compound is frequently used in organic chemistry research to explore new synthetic pathways and molecular transformations.
  • Pharmacological Studies: It supports pharmacological studies by providing a foundation for synthesizing compounds with potential therapeutic applications.
  • Biochemical Applications: Its role in biochemical applications includes the study of molecular interactions and the development of bioactive molecules.

Brand TCI
CAS number 365996-30-1
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various pack sizes as per supplier specifications
Physical form Solid, crystalline powder
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its stability. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation is essential when working with this compound to minimize inhalation risks. It is important to store it separately from incompatible substances to avoid any potential chemical reactions. Regular inspection of storage conditions ensures the compound remains in optimal condition for use in research applications.

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