(R)-B-methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine

Base Information

• Chemical Name: (R)-B-methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine
• CAS No.: 155268-88-5
• Molecular Formula: C₂₁H₂₀BNO
• Molecular Weight: 313.207
• DSSTox Substance ID: DTXSID30454032
• Nikkaji Number: J806.005C
• Wikidata: Q72492234
• Mol file: 155268-88-5.mol

Synonyms:155268-88-5;(R)-B-methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine;(4R)-2-METHYL-4,5,5-TRIPHENYL-1,3,2-OXAZABOROLIDINE;SCHEMBL7596564;DTXSID30454032;AMY14817;AKOS015902032;2-Methyl-4alpha,5,5-triphenyl-1,3,2-oxazaborolidine

Chemical Property of (R)-B-methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine

Chemical Property:

• Boiling Point: 405.339 °C at 760 mmHg
• Flash Point: 198.942 °C
• PSA: 21.26000
• Density: 1.13g/cm³
• LogP: 4.73810
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 313.1637944
• Heavy Atom Count: 24
• Complexity: 379

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: B1(NC(C(O1)(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4)C
• Isomeric SMILES: B1(N[C@@H](C(O1)(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4)C

Technology Process of (R)-B-methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine

There total 1 articles about (R)-B-methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

Trimethylboroxine (823-96-1) + (R)-(+)-2-amino-1,1,2-triphenylethanol (60539-17-5,79868-79-4,129704-13-8) → (4R)-2-methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine (155268-88-5)

Guidance literature:

In toluene; at 20 ℃; for 1h;

DOI:10.1021/jo701509r

upstream raw materials:

Trimethylboroxine

(R)-(+)-2-amino-1,1,2-triphenylethanol