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TCI

CAS 66674-16-6

N-Carbobenzoxy-L-alaninol TCI C2629

N-Carbobenzoxy-L-alaninol TCI C2629

Chemical Identity

Other names
N-Cbz-L-alaninol · (S)-N-Cbz-2-Amino-1-propanol · N-Benzyloxycarbonyl-L-alaninol · (S)-N-Benzyloxycarbonyl-2-Amino-1-propanol
CAS No.
66674-16-6
Formula
C11H15NO3
Molecular weight
209.25 g/mol
Purity
>98.0%(HPLC)(N)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
benzyl N-[(2S)-1-hydroxypropan-2-yl]carbamate
SMILES
CC(CO)NC(=O)OCC1=CC=CC=C1
InChIKey
AFPHMHSLDRPUSM-VIFPVBQESA-N
MDL
MDL00672530
PubChem
CID 10262499
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TCI C2629 66674-16-6 N-Carbobenzoxy-L-alaninol is a chemical compound widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in laboratories where precise control over stereochemistry is essential. It is particularly valuable in the development of bioactive compounds, as its chiral nature allows for the creation of enantiomerically pure products. Its importance is evident in both academic and industrial research settings, where it supports the synthesis of pharmaceuticals and other specialized chemicals.

The compound is known for its chemical stability and controlled reactivity, making it a preferred choice for researchers. Its well-defined molecular structure ensures consistency in experimental outcomes, which is vital for reproducibility in scientific studies. The availability of this compound in a solid form further enhances its usability, as it simplifies handling and storage. These properties make it a reliable reagent for a variety of chemical reactions, especially those requiring high precision.

In Indonesian laboratories, N-Carbobenzoxy-L-alaninol is commonly used in research related to the synthesis of bioactive compounds. It is a key component in the development of new drugs and pharmaceuticals, supporting both academic institutions and research centers. Its application in organic chemistry research underscores its importance in advancing scientific knowledge and innovation in the field.

  • Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, essential in pharmaceutical research for drug development.
  • Chiral Building Blocks: It serves as a fundamental component in the construction of complex molecular structures with defined stereochemistry.
  • Organic Chemistry Research: Its stability and reactivity make it a preferred reagent for various synthetic pathways in organic chemistry.
  • Drug Development: It is widely used in the synthesis of bioactive compounds, supporting the creation of new therapeutic agents.
  • Academic Research: It is a valuable tool for teaching and research in universities and research institutions focusing on chemical synthesis.

Brand TCI
CAS number 66674-16-6
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from direct light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical stability, it does not require refrigeration but should be protected from humidity. In laboratory settings, it is important to handle it with care, using appropriate personal protective equipment. Proper labeling and storage conditions ensure the compound remains effective for its intended applications. Always ensure the workspace is clean and free from potential chemical interactions.

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