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19999-87-2

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19999-87-2 Usage

Reaction

An approach to five-membered lactams from aliphatic amides and terminal acetylenes by nickel catalysis. Synthesis of biaryls through nickel-catalyzed Suzuki-Miyaura coupling of amides by carbon-nitrogen bond cleavage. Ni-catalyzed borylation of aryl fluorides via C-F cleavage. Nickeland palladium–catalyzed coupling of aryl fluorosulfonates with aryl boronic acids enabled by sulfuryl fluoride. Nickel-catalyzed one-pot synthesis of biaryls from phenols and arylboronic acids via C-O activation using TCT reagents.

Uses

Catalyst for:Dehydrobrominative polycondensationArylation reactionsCross-couplingSuzuki-miyaura cross-coupling reactionsKumada coupling of diaryl sulfates with Grignard reagentsOlefin dimerization

Check Digit Verification of cas no

The CAS Registry Mumber 19999-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,9 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19999-87:
(7*1)+(6*9)+(5*9)+(4*9)+(3*9)+(2*8)+(1*7)=192
192 % 10 = 2
So 19999-87-2 is a valid CAS Registry Number.
InChI:InChI=1/2C18H33P.2ClH.Ni/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h2*16-18H,1-15H2;2*1H;/q;;;;+2/p-2

19999-87-2 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (B3534)  Bis(tricyclohexylphosphine)nickel(II) Dichloride  >95.0%(T)

  • 19999-87-2

  • 1g

  • 540.00CNY

  • Detail
  • TCI America

  • (B3534)  Bis(tricyclohexylphosphine)nickel(II) Dichloride  >95.0%(T)

  • 19999-87-2

  • 5g

  • 1,520.00CNY

  • Detail
  • Aldrich

  • (708526)  Bis(tricyclohexylphosphine)nickel(II)dichloride  97%

  • 19999-87-2

  • 708526-1G

  • 478.53CNY

  • Detail

19999-87-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name dichloronickel,tricyclohexylphosphane

1.2 Other means of identification

Product number -
Other names Dichlorobis(tricyclohexylphosphine)nickel(II)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19999-87-2 SDS

19999-87-2Relevant articles and documents

Catalyst and application thereof in synthesis of aromatic fluorine compounds

-

Paragraph 0027-0029, (2020/11/10)

The invention belongs to the field of catalyst preparation and application, and particularly relates to a catalyst and application thereof in synthesis of aromatic fluorine compounds. The nickel catalyst is dichloro-bis-(tri-cyclohexylphosphine) nickel, and the molecular formula of the nickel catalyst is Ni (Py3) 2Cl2. The nickel catalyst is applied to catalyzing inorganic fluoride to replace aromatic chloride to synthesize fluoride. The catalyst has the advantages of easily available reagents, simple catalyst synthesis, simple operation conditions, low reaction temperature, high reaction yield and less time consumption.

A broadly applicable strategy for entry into homogeneous nickel(0) catalysts from air-stable nickel(II) complexes

Standley, Eric A.,Smith, Stacey J.,Mueller, Peter,Jamison, Timothy F.

supporting information, p. 2012 - 2018 (2014/05/20)

A series of air-stable nickel complexes of the form L2Ni(aryl) X (L = monodentate phosphine, X = Cl, Br) and LNi(aryl)X (L = bis-phosphine) have been synthesized and are presented as a library of precatalysts suitable for a wide variety of nickel-catalyzed transformations. These complexes are easily synthesized from low-cost NiCl2·6H2O or NiBr 2·3H2O and the desired ligand followed by addition of 1 equiv of Grignard reagent. A selection of these complexes were characterized by single-crystal X-ray diffraction, and an analysis of their structural features is provided. A case study of their use as precatalysts for the nickel-catalyzed carbonyl-ene reaction is presented, showing superior reactivity in comparison to reactions using Ni(cod)2. Furthermore, as the precatalysts are all stable to air, no glovebox or inert-atmosphere techniques are required to make use of these complexes for nickel-catalyzed reactions.

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