dichlorotriphenylstibane

• ChemBase ID: 111504
• Molecular Formular: C18H15Cl2Sb
• Molecular Mass: 423.9777
• Monoisotopic Mass: 421.95889584
• SMILES: Cl[Sb](Cl)(c1ccccc1)(c1ccccc1)c1ccccc1
• Canonical SMILES: Cl[Sb](c1ccccc1)(c1ccccc1)(c1ccccc1)Cl
• InChI: InChI=1S/3C6H5.2ClH.Sb/c3*1-2-4-6-5-3-1;;;/h3*1-5H;2*1H;/q;;;;;+2/p-2
• InChIKey: PDGPVQHGCLPCES-UHFFFAOYSA-L

NAMES AND DATABASE IDS

Names

• IUPAC name: dichlorotriphenylstibane
• IUPAC Traditional name: antimony, dichlorotriphenyl-
• Synonyms: TRIPHENYL ANTIMONY DICHLORIDE; Triphenylstibine dichloride; Triphenylantimony(V) dichloride; Dichlorotriphenylantimony(V); NSC 179782; NSC 432; 三苯基二氯化锑; 三苯基二氯化锑(V)

Database IDs

• CAS Number: 594-31-0
• EC Number: 209-834-1
• MDL Number: MFCD00013598
• PubChem SID: 162096689; 24848199
• PubChem CID: 11662

CALCULATED PROPERTIES

• H Acceptors: 0
• H Donor: 0
• LogD (pH = 5.5): 6.0812
• LogD (pH = 7.4): 6.0812
• Log P: 6.0812
• Molar Refractivity: 88.6955 cm^3
• Polarizability: 38.922596 Å^3
• Polar Surface Area: 0.0 Å^2
• Rotatable Bonds: 3
• Lipinski's Rule of Five: false

PROPERTIES

Physical Property

• Melting Point: 143-145 °C(lit.)

Safety Information

• RTECS: CC5095000
• European Hazard Symbols: Nature polluting (N); Harmful (Xn)
• UN Number: 2923
• German water hazard class: 2
• Hazard Class: 8
• Packing Group: 2
• Risk Statements: 20/22-51/53; R:20/22-51/53
• Safety Statements: 61; S:61
• GHS Pictograms: GHS07; GHS09
• GHS Signal Word: Warning
• GHS Hazard statements: H302-H332-H411
• GHS Precautionary statements: P273
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Faceshields, Gloves
• RID/ADR: UN 2923 8/PG 2

Product Information

• Purity: 99%
• Linear Formula: (C6H5)3SbCl2

DETAILS

MP Biomedicals - 05219546

MP Biomedicals Rare Chemical collection

Sigma Aldrich - 135097

Packaging
5 g in glass bottle
Application
Catalyst for:
• Regioselective cycloaddition of aziridines with heterocumulenes1
• Reaction of epoxides with carbon dioxide2Reactant for synthesis of:
• Tetraphenylantimony compounds with arylcarbonyloxy moieties3
• Symmetrical 24-membered macrocyclic organoantimony(V) complexes4Reactant for oxidation5 and Suzuki-type cross couplings6