Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
41073
CAS Number:
850661-66-4
(S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine (ca. 6% in Toluene, ca. 0.1mol/L)
Purity:
≥ 98%
Documents
$363.84 /10ML
Pack Size Availability Price
Request Bulk Quote
Product Information

(S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine is a specialized compound known for its unique boron-containing structure, which enhances its reactivity and selectivity in various chemical reactions. This compound is particularly valuable in asymmetric synthesis, where it serves as a chiral catalyst, facilitating the production of enantiomerically pure compounds. Its ability to stabilize transition states makes it an excellent choice for researchers and industry professionals looking to optimize reaction conditions in organic synthesis.

In addition to its role in catalysis, this compound has shown promise in medicinal chemistry, particularly in the development of pharmaceuticals that require precise stereochemistry. Its compatibility with various solvents, such as toluene, allows for flexibility in experimental setups, making it a preferred choice in laboratories focused on innovative chemical research. With its unique properties and practical applications, (S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine stands out as a valuable tool for advancing synthetic methodologies and enhancing the efficiency of chemical processes.

CAS Number
850661-66-4
Purity
≥ 98%
Molecular Formula
C34H32BNO
Molecular Weight
481.45
MDL Number
MFCD23143154
PubChem ID
73409913
Density
0.93 g/mL
Appearance
Colorless to slightly yellow liquid
Refractive Index
n20D 1.50
Conditions
Store at RT
General Information
CAS Number
850661-66-4
Purity
≥ 98%
Molecular Formula
C34H32BNO
Molecular Weight
481.45
MDL Number
MFCD23143154
PubChem ID
73409913
Density
0.93 g/mL
Appearance
Colorless to slightly yellow liquid
Refractive Index
n20D 1.50
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a chiral catalyst in asymmetric synthesis, enabling the production of enantiomerically pure compounds, which is crucial in pharmaceuticals for developing effective drugs with fewer side effects.
  • Organocatalysis: It is employed in organocatalytic reactions, providing a more environmentally friendly alternative to traditional metal catalysts, thus reducing toxic waste in chemical processes.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanocomposites, enhancing their properties like strength and thermal stability for applications in electronics and packaging.
  • Drug Development: Its role in drug discovery includes facilitating the synthesis of complex organic molecules, which can lead to new therapeutic agents, particularly in cancer and infectious diseases.
  • Research in Green Chemistry: This chemical contributes to green chemistry initiatives by enabling reactions that minimize energy consumption and reduce hazardous byproducts, aligning with sustainable practices in chemical manufacturing.

Citations