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Catalog Number:
18848
CAS Number:
150482-72-7
S-3-Amino-2(benzylamino)propan-1-ol
Purity:
≥ 95% (NMR)
Documents
$153.63 /100MG
Pack Size Availability Price
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Product Information

(S)-3-Amino-2(benzylamino)propan-1-ol is a versatile compound widely recognized for its applications in pharmaceutical and biochemical research. This chiral amino alcohol serves as a crucial building block in the synthesis of various biologically active molecules, particularly in the development of pharmaceuticals targeting neurological and metabolic disorders. Its unique structure allows for the formation of diverse derivatives, enhancing its utility in medicinal chemistry.

Researchers value (S)-3-Amino-2(benzylamino)propan-1-ol for its ability to facilitate the design of compounds with improved efficacy and selectivity. Its role in asymmetric synthesis makes it an essential reagent for creating enantiomerically pure substances, which is vital in drug development. Additionally, its compatibility with various reaction conditions broadens its application scope, making it a preferred choice for chemists seeking reliable and effective intermediates in their synthetic pathways.

CAS Number
150482-72-7
Purity
≥ 95% (NMR)
Molecular Formula
C10H16N2O
Molecular Weight
180.25
MDL Number
MFCD06658298
PubChem ID
15755072
Appearance
Oil
Conditions
Store at 0-8 °C
General Information
CAS Number
150482-72-7
Purity
≥ 95% (NMR)
Molecular Formula
C10H16N2O
Molecular Weight
180.25
MDL Number
MFCD06658298
PubChem ID
15755072
Appearance
Oil
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

(S)-3-Amino-2(benzylamino)propan-1-ol 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 drugs targeting neurological disorders.
  • Biochemical Research: It is used in studies related to enzyme inhibition and protein interactions, helping researchers understand complex biological processes.
  • Chiral Synthesis: Its chiral nature makes it valuable in asymmetric synthesis, allowing for the creation of enantiomerically pure compounds, which are crucial in drug formulation.
  • Material Science: This chemical is explored for its potential in creating novel materials with specific properties, such as improved solubility and stability in various environments.
  • Diagnostic Applications: It is investigated for use in diagnostic assays, particularly in the detection of certain biomolecules, enhancing the accuracy of medical tests.

Citations