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709042

Sigma-Aldrich

[1,3-双(2,6-二异丙基苯基)咪唑-2-亚基]氯[3-苯基烯丙基]钯(II)

Umicore, 95%

同義詞:

CX 31

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About This Item

經驗公式（希爾表示法）:
C36H45ClN2Pd
CAS號碼:
884879-23-6
分子量：:
647.63
MDL號碼:
MFCD11045095
分類程式碼代碼:
12161600
PubChem物質ID:
329762845
NACRES:
NA.22
暫時無法取得訂價和供貨情況

化驗

95%

形狀

powder

反應適用性

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst

mp

205-208 °C

SMILES 字串

[CH2][CH][CH]c1ccccc1.CC(C)c2cccc(C(C)C)c2N3C=CN(\C3=[Pd]/Cl)c4c(cccc4C(C)C)C(C)C

InChI

1S/C27H36N2.C9H9.ClH.Pd/c1-18(2)22-11-9-12-23(19(3)4)26(22)28-15-16-29(17-28)27-24(20(5)6)13-10-14-25(27)21(7)8;1-2-6-9-7-4-3-5-8-9;;/h9-16,18-21H,1-8H3;2-8H,1H2;1H;/q;;;+1/p-1

InChI 密鑰

RWGNZUQSYXTZIX-UHFFFAOYSA-M

相關類別

應用

  • Catalyst for Suzuki coupling[1] (eq. 1)
  • Catalyst for Buchwald-Hartwig amination reaction[2] (eq. 2)
Catalyst for:
  • Suzuki-Miyaura couplings
  • Buchwald-Hartwig couplings

法律資訊

Product of Umicore

Additional information available at www.pmc.umicore.com

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

從最近期的版本中選擇一個：

分析證明 (COA)

Lot/Batch Number
MKCT8211
MKCN7993
MKBR3468V
MKBQ9686V
MKBC1754V

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Nicolas Marion et al.
Journal of the American Chemical Society, 128(12), 4101-4111 (2006-03-23)
A series of (NHC)Pd(R-allyl)Cl complexes [NHC: IPr = N,N'-bis(2,6-diisopropylphenyl)imidazol-2-ylidene, SIPr = N,N'-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazol-2-ylidene; R = H, Me, gem-Me2, Ph] have been synthesized and fully characterized. When compared to (NHC)Pd(allyl)Cl, substitution at the terminal position of the allyl scaffold favors a more
Bruce H Lipshutz et al.
Organic letters, 10(7), 1333-1336 (2008-03-14)
Use of a dilute aqueous solution containing a nonionic amphiphile allows efficient Suzuki-Miyaura cross-couplings of arylboronic acids with a wide array of aryl halides and pseudohalides, including sterically hindered and lipophilic substrates, in most cases at room temperature.
Oscar Navarro et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(19), 5142-5148 (2006-04-22)
The use of second-generation [(NHC)Pd(R-allyl)Cl] complexes for Suzuki-Miyaura and Buchwald-Hartwig cross-coupling reactions involving heteroaromatic halides at room temperature is reported. The first examples of room temperature Suzuki-Miyaura cross-coupling of deactivated aryl chlorides with alkenyl boronic acids are also disclosed. Terminal

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