Chloro[tri(o-tolyl)phosphine]gold(I)
Chloro[tri(o-tolyl)phosphine]gold(I) Basic information
- Product Name:
- Chloro[tri(o-tolyl)phosphine]gold(I)
- Synonyms:
-
- Chloro[tri(o-tolyl)phosphine]gold(I),95%
- Chloro[tri(o-tolyl)phosphine]gold(I)
- (Tri-o-tolylphosphine)gold chloride
- Chloro(tri(2-methylphenyl)phosphine)gold
- Chloro(tri-o-tolylphosphine)gold
- Chloro(tris(2-tolyl)phosphine)gold
- Chloro[tris(2-methylphenyl)phosphine]gold
- Chloro[tris(o-methylphenyl)phosphine]gold
- CAS:
- 83076-07-7
- MF:
- C21H20AuClP+
- MW:
- 535.776811
- Product Categories:
-
- Au
- Mol File:
- 83076-07-7.mol
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Chloro[tri(o-tolyl)phosphine]gold(I) Chemical Properties
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- solid
- Appearance
- White to off-white Solid
- InChI
- 1S/C21H21P.Au.ClH/c1-16-10-4-7-13-19(16)22(20-14-8-5-11-17(20)2)21-15-9-6-12-18(21)3;;/h4-15H,1-3H3;;1H/q;+1;/p-1
- InChIKey
- VECXLHSTZNCQLD-UHFFFAOYSA-M
- SMILES
- Cl[Au].Cc1ccccc1P(c2ccccc2C)c3ccccc3C
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Chloro[tri(o-tolyl)phosphine]gold(I) Usage And Synthesis
Uses
Gold Catalysts — 21st Century ′Gold Rush′
Catalyst for:
- Alkylation of silyl enol ethers with orthoalkynylbenzoic acid esters
- Cycloisomerization
- Cyclization of 1,6-enynes
- Tandem [3,3]-sigmatropic rearrangement-cycloisomerization cascade
- Cycloaddition of enyne derivatives with aryl alkynes or alkenes
reaction suitability
core: gold
reagent type: catalyst
Chloro[tri(o-tolyl)phosphine]gold(I)Supplier
Energy Chemical
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Shanghai Jian Chao Chemical Technology Co., Ltd.
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- 150-2103-5486 18017383231
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