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Catalog Number:
39488
CAS Number:
78603-95-9
(S)-(-)-2-Amino-3-methyl-1,1-diphenyl-1-butanol
Purity:
≥ 98% (Assay by titration, Chiral HPLC)
Documents
$174.96 /1G
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Product Information

(S)-(-)-2-Amino-3-methyl-1,1-diphenyl-1-butanol is a chiral amino alcohol that plays a significant role in the synthesis of pharmaceuticals and fine chemicals. This compound is recognized for its ability to act as a versatile building block in asymmetric synthesis, particularly in the production of various biologically active molecules. Its unique structure allows for the introduction of chirality, making it invaluable in the development of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for ensuring efficacy and safety in drug formulations.

Researchers and industry professionals utilize (S)-(-)-2-Amino-3-methyl-1,1-diphenyl-1-butanol in the synthesis of chiral intermediates and active pharmaceutical ingredients (APIs). Its application extends to the production of antihypertensive agents and other therapeutic compounds, showcasing its importance in medicinal chemistry. The compound's high purity and stability make it an excellent choice for rigorous laboratory applications, ensuring reliable results in various chemical reactions.

CAS Number
78603-95-9
Purity
≥ 98% (Assay by titration, Chiral HPLC)
Molecular Formula
C17H21NO
Molecular Weight
255.36
MDL Number
MFCD01318248
PubChem ID
3808242
Melting Point
96 - 101 °C
Appearance
White or off-white crystalline powder
Optical Rotation
[α]20D = -142 ° (C=1 in CHCl3)
Conditions
Store at 2 - 8 °C
General Information
CAS Number
78603-95-9
Purity
≥ 98% (Assay by titration, Chiral HPLC)
Molecular Formula
C17H21NO
Molecular Weight
255.36
MDL Number
MFCD01318248
PubChem ID
3808242
Melting Point
96 - 101 °C
Appearance
White or off-white crystalline powder
Optical Rotation
[α]20D = -142 ° (C=1 in CHCl3)
Conditions
Store at 2 - 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)-(-)-2-Amino-3-methyl-1,1-diphenyl-1-butanol 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.
  • Chiral Catalysis: Its chiral properties make it valuable in asymmetric synthesis, allowing for the production of enantiomerically pure compounds, which are crucial in the pharmaceutical industry.
  • Research in Organic Chemistry: It is frequently used in organic synthesis to explore new reaction pathways and mechanisms, helping researchers develop innovative chemical processes.
  • Biochemical Studies: The compound is utilized in studies investigating enzyme interactions and metabolic pathways, providing insights into biological processes and drug metabolism.
  • Material Science: Its unique structure can be applied in the development of new materials with specific properties, such as enhanced stability or reactivity, beneficial for various industrial applications.

Citations