Bromotris(dimethylamino)phosphonium hexafluorophosphate

Base Information

• Chemical Name: Bromotris(dimethylamino)phosphonium hexafluorophosphate
• CAS No.: 50296-37-2
• Molecular Formula: C6H18BrF6N3P2
• Molecular Weight: 388.07
• Hs Code.: 29299090
• European Community (EC) Number: 634-865-6
• DSSTox Substance ID: DTXSID90436970
• Mol file: 50296-37-2.mol

Synonyms:50296-37-2;Bromotris(dimethylamino)phosphonium hexafluorophosphate;BroP;Bromotris(dimethylamino)phosphonium hexafluorophosphate(V);bromo-tris(dimethylamino)phosphanium;hexafluorophosphate;Bromotris(N-methylmethanaminato)-phosphorus hexafluorophosphate;Bromotris(dimethylamino)phosphoniumHexafluorophosphate;bromo-tris(dimethylamino)phosphonium hexafluorophosphate;SCHEMBL21055822;DTXSID90436970;XELPBWPBGHCIKX-UHFFFAOYSA-N;MFCD00191864;AKOS015833788;AM83813;CS-W011739;AC-24864;B3838;FT-0658922;A828054;J-519953;bromanyl-tris(dimethylamino)phosphanium hexafluorophosphate;Bromotris(dimethylamino)phosphonium hexafluorophosphate, 98%;bromotris(dimethylamino)phosphanium;hexafluoro-??-phosphanuide;Bromotris(dimethylamino)phosphonium hexafluorophosphate(V)(BROP)

Chemical Property of Bromotris(dimethylamino)phosphonium hexafluorophosphate

Chemical Property:

• Melting Point: >300 °C(lit.)
• PSA: 36.90000
• LogP: 5.12610
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• Sensitive.: Light Sensitive
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 3
• Exact Mass: 387.00635
• Heavy Atom Count: 18
• Complexity: 168

Purity/Quality:

99% ^*data from raw suppliers

Bromotris(dimethylamino)phosphonium Hexafluorophosphate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 45-34
• Safety Statements: 53-26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C)[P+](N(C)C)(N(C)C)Br.F[P-](F)(F)(F)(F)F
• Uses: Reagent for: Conjugate addition of nitroalkanes to an acrylate equivalent A novel polymer supported approach to nucleoside modification Asymmetric hydrogenations Peptide coupling Pyrrolidine hydroxylation Synthesis of cyclic PNA-based compound directed against HIV-1 TAR RNA