| Weight | 280.379 g/mol |
|---|---|
| Formula | C12H9PS3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
Tris(2-thienyl)phosphine (24171-89-9)
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- Two modes of C-H bond activation of tris(2-thienyl)phosphine in trinuclear osmium carbonyl clusters (Journal of Organometallic Chemistry, 2007)
- Tris[tri(2thienyl)phosphine]palladium as the catalyst precursor for thiophenebased SuzukiMiyaura crosscoupling and polycondensation (Journal of Polymer Science Part A, 2008)
- Reaction of Tris(2-thienyl)phosphine with Dirhodium(II) Acetate. Orthometalation of a Heteroaromatic -System and an Unusual Ring Rearrangement (Organometallics, 2003)
- Crystal Structures and Spectroscopic Properties of trans-N,P-[Pt(ppy)(Pmor3)Cl] and trans-N,P-[Pt(tpy)(Pmor3)Cl].CH3CN [ppy = N,C'-chelated 2-phenylpyridinate, tpy = N,C'-Chelated 2-(2'-thienyl)pyridinate, Pmor3 = tris(morpholino)phosphine]. (Acta Chemica Scandinavica, 1996)
- TRIS[(5-CHLORO-2-THIENYL)METHYL] PHOSPHINE OXIDE FROM ELEMENTAL PHOSPHORUS AND 2-CHLORO-5-(CHLOROMETHYL) THIOPHENE (Phosphorus Sulfur and Silicon and The Related Elements, 2001)
- Formation of Alkyne Bridged Multicobalt Carbonyl Complexes with Tris(2-Thienyl)Phosphine or Bis(Trimethylsilylethynyl)Phenylphosphine Ligand (Journal of The Chinese Chemical Society, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CSC(=C1)P(C2=CC=CS2)C3=CC=CS3
-
InChIKeyKUCPTMZJPDVWJL-UHFFFAOYSA-N
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Tris(2-thienyl)phosphine
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