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199982

Sigma-Aldrich

三(三苯基膦)氯化铑(I)

别名:

NSC 124140, RhCl (PPh 3 ) 3, Wilkinson 催化剂, 三(三苯膦基)氯化铑(I)

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About This Item

线性分子式:
[(C6H5)3P]3RhCl
CAS号:
14694-95-2
分子量:
925.22
Beilstein:
4581440
EC號碼:
238-744-5
MDL號碼:
MFCD00010016
分類程式碼代碼:
12161600
PubChem物質ID:
24851950
NACRES:
NA.22

品質等級

200

反應適用性

core: rhodium
reagent type: catalyst

SMILES 字串

Cl[Rh].c1ccc(cc1)P(c2ccccc2)c3ccccc3.c4ccc(cc4)P(c5ccccc5)c6ccccc6.c7ccc(cc7)P(c8ccccc8)c9ccccc9

InChI

1S/3C18H15P.ClH.Rh/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;/h3*1-15H;1H;/q;;;;+1/p-1

InChI 密鑰

IXAYKDDZKIZSPV-UHFFFAOYSA-M

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相关类别

一般說明

三（三苯基膦）氯化铑（I）在Heck反应中被用作脱羧试剂和协同催化剂。

應用

硅氢化催化剂

用于许多有机反应的催化剂，包括：
  • 化学选择性烯丙基烷基化
  • Si-H 键的化学计量活化 与硅氢化反应
  • 烯烃分子间和分子内加氢酰化（含助催化剂）
  • 二有机硅烷的聚合

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H317,H413

危險分類

Aquatic Chronic 4 - Skin Sens. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

個人防護裝備

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCG4968
BCCG1374
BCCD6919
BCCD6917
BCCB0258

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The Journal of Organic Chemistry, 57, 5075-5075 (1992)
Chemical Reviews, 91, 1179-1179 (1991)
Effect of catalytic hydrogenation of cellular lipid and fatty acid on the susceptibility of tumor cells to humoral immune killing.
S I Schlager
Methods in enzymology, 73(Pt B), 191-199 (1981-01-01)
V P Shevchenko et al.
Bioorganicheskaia khimiia, 36(2), 283-288 (2010-06-10)
1,2-Tritium-labeled 3-(O-carboxypropyl)- and 3-(O-carbomethoxypropyl)-oximes of 6alpha-methyl-16alpha,17alpha-cyclohexanopregn-4-ene-3,20-diones were obtained by the homogeneous catalytic hydrogenation of 1,2-dehydroprecursors with gaseous tritium and the subsequent separation of the resulting mixtures by HPLC. The specific radioactivities of 50-55 Ci/mmol were prepared using tris-(triphenylphosphine)-rhodium chloride.
P Andrew Evans et al.
Journal of the American Chemical Society, 124(30), 8782-8783 (2002-07-26)
Transition metal-catalyzed cycloaddition reactions represent powerful methods for the construction of complex polycyclic systems. We have developed a new intermolecular metal-catalyzed [4 + 2 + 2] cycloaddition of heteroatom-tethered enyne derivatives with 1,3-butadiene. This study demonstrates that excellent selectivity can
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