(2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine | CAS No. 146476-38-2

(2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine

Basic Information

CAS Number

146476-38-2

Molecular Formula

C21H22NP

Molecular Weight

319.39 g/mol

AD

Basic Physical Properties

c1ccc(cc1)C[C@@H](CP(c2ccccc2)c3ccccc3)N

InChI

InChI=1S/C21H22NP/c22-19(16-18-10-4-1-5-11-18)17-23(20-12-6-2-7-13-20)21-14-8-3-9-15-21/h1-15,19H,16-17,22H2/t19-/m0/s1

InChIKey

SIOSCJGIYDRXMO-IBGZPJMESA-N

LogP

3.689300000000001

Topological Polar Surface Area

26.02 Ų

Hydrogen Bond Donor/Acceptor

2 / 1

Complexity

296

Synonyms & References

English

  • (S)-1-(diphenylphosphino)-3-phenylpropan-2-aMine
  • (αS)-α-[(Diphenylphosphino)methyl]benzeneethanamine
  • [(2S)-2-Amino-3-phenylpropyl]diphenylphosphine
  • (2S)-1-diphenylphosphanyl-3-phenylpropan-2-amine
  • (alphaS)-alpha-[(Diphenylphosphino)methyl]benzeneethanamine
  • (
  • AS)-
  • A-[(Diphenylphosphino)methyl]benzeneethanamine
  • (S)-1-(Diphenylphosphanyl)-3-phenylpropan-2-amine
  • Benzeneethanamine, α-[(diphenylphosphino)methyl]-, (αS)-

FAQ

What are the physical and chemical properties of (2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine (CAS: 146476-38-2)?

The compound (2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine (CAS: 146476-38-2) is a clear to slightly yellow liquid at room temperature. It has a molecular weight of approximately 408.4 g/mol and a high solubility in organic solvents such as THF and DMSO. This compound is known for its reactivity in organophosphorus chemistry and its ability to act as a ligand in transition metal catalysis.

How is (2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine (CAS: 146476-38-2) typically synthesized?

The compound (2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine (CAS: 146476-38-2) is typically synthesized via a multi-step process involving the coupling of diphenylphosphine and 3-phenyl-2-propanamine. The reaction is catalyzed by a strong base, and the product is obtained with good yield and high selectivity. The exact conditions can vary, but a common method involves using potassium hexafluorophosphate in the presence of a polar aprotic solvent.

What industries use (2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine (CAS: 146476-38-2)?

The compound (2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine (CAS: 146476-38-2) is primarily used in the pharmaceutical and chemical industries. It serves as a key ligand in transition metal catalysis, particularly in the development of chiral catalysts for the synthesis of pharmaceuticals and agrochemicals. The compound is also utilized in the production of polymers and as a ligand in organophosphorus chemistry.

What precautions should be taken when handling (2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine (CAS: 146476-38-2)?

When handling (2S)-1-(Diphenylphosphino)-3-phenyl-2-propanamine (CAS: 146476-38-2), it is important to use appropriate personal protective equipment (PPE), including gloves, goggles, and a lab coat. The compound should be stored in a cool, dry place away from heat sources and in a fume hood during use. In case of spillage, it is recommended to use absorbent material and dispose of it according to local regulations. Always consult the safety data sheet (SDS) for detailed handling and disposal instructions.

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