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Bis(acetonitrile)dichloropalladium(II)

CAS No.
14592-56-4
Chemical Name:
Bis(acetonitrile)dichloropalladium(II)
Synonyms
BIS(ACETONITRILE)PALLADIUM(II) DICHLORIDE;(MeCN)2PdCl2;bis(acetonitrile)dichloropalladium;Palladium, bis(acetonitrile)dichloro-;TRANS-BIS(ACETONITRILE)PALLADIUM(II) CHLORIDE;DICHLOROBIS(ACETONITRILE)PALLADIUM(II);BIS(ACETONITRILE)PALLADIUM(II) CHLORIDE;e)dichL;Bis(acetonitriL;Bis(Acetonitrile)Pd(II)
CBNumber:
CB8245652
Molecular Formula:
C4H6Cl2N2Pd
Molecular Weight:
259.43
MDL Number:
MFCD00013122
MOL File:
14592-56-4.mol
MSDS File:
SDS
Last updated:2023-08-15 17:37:19

Bis(acetonitrile)dichloropalladium(II) Properties

Melting point 300 °C
storage temp. Inert atmosphere,Room Temperature
solubility Soluble in acetonitrile, acetone, chloroform
form Fine Crystalline Powder
color Orange to rust-brown
Water Solubility insoluble
CAS DataBase Reference 14592-56-4(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H301+H311+H331
Precautionary statements  P280-P301+P310+P330-P302+P352+P312-P304+P340+P311
Hazard Codes  T,Xn
Risk Statements  23/24/25-36/37/38-20/21/22
Safety Statements  16-27-36/37-45-36-26
RIDADR  UN 3077 9/PG 3
WGK Germany  3
TSCA  No
HazardClass  6.1
PackingGroup  III
HS Code  28439090
NFPA 704
1
3 0

Bis(acetonitrile)dichloropalladium(II) price More Price(53)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 225657 Bis(acetonitrile)dichloropalladium(II) 99% 14592-56-4 500mg $77 2024-03-01 Buy
Sigma-Aldrich 225657 Bis(acetonitrile)dichloropalladium(II) 99% 14592-56-4 5g $502 2024-03-01 Buy
TCI Chemical B1676 Bis(acetonitrile)palladium(II) Dichloride >98.0%(T) 14592-56-4 1g $279 2024-03-01 Buy
TCI Chemical B1676 Bis(acetonitrile)palladium(II) Dichloride >98.0%(T) 14592-56-4 5g $1046 2024-03-01 Buy
Alfa Aesar 010002 Bis(acetonitrile)dichloropalladium(II), Pd 40.5% 14592-56-4 1g $123 2023-06-20 Buy
Product number Packaging Price Buy
225657 500mg $77 Buy
225657 5g $502 Buy
B1676 1g $279 Buy
B1676 5g $1046 Buy
010002 1g $123 Buy

Bis(acetonitrile)dichloropalladium(II) Chemical Properties,Uses,Production

Reaction

  1. Catalyst for the cyclization of δ-acetylenic carboxylic acids to butenolides.
  2. Catalyst for the aza-Michael reaction of carbamates with enones.
  3. Catalyst for the rearrangement of allylic imidates to allylic amides.
  4. Catalyst for the Nazarov cyclization of α-alkoxy dienones.
  5. Catalyst for the diamination of conjugated dienes.
  6. Three component Michael addition, cyclization, cross-coupling reaction.
  7. C-H activation of indoles.
  8. Catalyst used for the direct C-H arylation of isoxazoles at the 5 position.
Reactions of 14592-56-4_1
Reactions of 14592-56-4_2

Chemical Properties

Light yellow to Brown powder to crystaline.

Physical properties

Bis(acetonitrile)dichloropalladium(II) is a yellow-brown solid that is soluble in organic solvents. It is a reagent and a catalyst for reactions that require soluble Pd(II).The compound is similar to bis(benzonitrile)palladium dichloride. 

Uses

It is used as a catalyst in an ether-directed aza-Claisen rearrangement. Also used in cyclization and cross-coupling reactions. It is applied for olefin isomerization, preparation of acetals and hemiacetal esters.

Uses

suzuki reaction

Uses

Catalyst used in an ether-directed aza-Claisen rearrangement.

Application

Synthesis of Oxindoles
Synthesis of Oxindoles.gif
To a dried screw-cap vial is added anilide (0.3 mmol), AgOCOCF3 (132.5 mg, 0.6 mmol), Bis(acetonitrile)dichloropalladium(II) (3.5 mg, 0.015 mmol) and chlorobenzene. The reaction mixture is stirred at 100-120 °C for 3-12 h in a pre-heated oil bath. After cooling to room temperature, the reaction is diluted with EtOAc and filtered with a glass filter. The filtrate is washed with 5% aqueous NaHCO3 and brine. The extract is dried over MgSO4 and concentrated in vacuo. The crude is purified by preparative TLC.

Preparation

Bis(acetonitrile)palladium dichloride is prepared by reacting two acetonitrile ligands and palladium(II) chloride.

General Description

This product has been enhanced for catalytic efficiency.

Bis(acetonitrile)dichloropalladium(II) Preparation Products And Raw materials

Global( 369)Suppliers
Supplier Tel Email Country ProdList Advantage
Wuhan Huahan Dingcheng New Material Technology Co., Ltd
+undefined-027-81388558 +undefined086-1878077615 huahandingcheng@sina.com China 342 58
Hebei Mojin Biotechnology Co., Ltd
+8613288715578 sales@hbmojin.com China 12456 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886 info@dakenam.com China 15928 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
AB PharmaTech,LLC
323-480-4688 United States 989 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Accela ChemBio Inc.
(+1)-858-699-3322 info@accelachem.com United States 19965 58

View Lastest Price from Bis(acetonitrile)dichloropalladium(II) manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Bis(acetonitrile)dichloropalladium(II) pictures 2023-08-15 Bis(acetonitrile)dichloropalladium(II)
14592-56-4
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
Bis(acetonitrile)dichloropalladium(II) pictures 2022-09-24 Bis(acetonitrile)dichloropalladium(II)
14592-56-4
US $0.00 / kg 1kg 99% 1000kg henan kanbei chemical co.,ltd
Bis(acetonitrile)dichloropalladium(II) pictures 2021-11-13 Bis(acetonitrile)dichloropalladium(II)
14592-56-4
US $10.00 / KG 1KG 99% 5tons Hebei Guanlang Biotechnology Co., Ltd.
PALLADIUM(II) CHLORIDE-DIACETONITRILE COMPLEX PALLADIUM-BIS-ACETONITRIL-DICHLORIDE PALLADIUM DICHLOROBIS(ACETONITRILE) TRANS-DICHLOROBIS(ACETONITRILE)PALLADIUM Bis(cyanomethyl)dichloropalladium(IV) Bis(acetonitrile)palladium(II) chloride,99% Bis(acetonitrile)dichloropalladium(Ⅱ) Dichlorobis(acetonitrile)palladiuM(II),98% (CH3CN)2PdCl2 Bis(acetonitrile)palladiuM(II) Bis(acetonitrile)palladiuM(II) chloride, 99% 500MG PalladiuM,bis(acetonitrile)dichloro- (8CI,9CI) Bis(acetonitrile)palladiuM(II) chloridel Bis(acetonitrile)-palladium(II) chloride (41% Pd) for synthesis DICHLOROBIS(ACETONITRILE)PALLADIUM(III) BIS(ACETONITRILE)DICHLOROPALLADATE (II) BIS(ACETONITRILE)DICHLOROPALLADIUM(II) bis (acetontrile) dichloropalladium (II) BIS(ACETONITRILE)DICHLOROPALLADIUM(II), 99.99% BIS(ACETONITRILE)DICHLOROPALLADIUM(II),99% TRANS-BIS(ACETONITRILE) DICHLOROPALLADIUM(II) BIS-(ACETONITRIL)DICHLOROPALLADIUM(II) Dichlorobis(acetonitrile)palladium(II),99% Palladium(II)chloro-bis(acetonitrile) DICHLOROBIS(ACETONITRILE)PALLADIUM(II) (41%PD) BIS(ACETONITRILE)PALLADIUM (II) CHLORIDE 99% BIS(ACETONITRILE)PALLADIUM()CHLORIDE Bis(acetonitrile)dichloropalladium(II), Pd 40.5% Trans-dichlorobis(acetonitrile)palladium(II) Can be used to form catalysts in situ by separate addition of ligand Bis(acetonitriL e)dichL PALLADIUM(2+) ION BIS(ACETONITRILE) DICHLORIDE Bis(acetonitrile)palladium(Ⅱ) chloride Acetonitrile - dichloropalladium (2:1) (II)Bis(acetonitrile)dichloropalladium(II) TRANS-BIS(ACETONITRILE)PALLADIUM(II) CHL Bis(acetonitrile)palladium(II) Dichloride > Bis(acetonitrile)dichloropalladium(II) ISO 9001:2015 REACH Bis(Acetonitrile)Pd(II) palladium(2+) bis(acetonitrile) dichloride Bis(Acetonitrile)Dichloropalladium (II) extrapure, 99%, ~41% Pd DICHLOROBIS (ACETONITRILE) PALLADIUM (II) For Synthesis TRANS-BIS(ACETONITRILE)PALLADIUM(II) CHLORIDE (MeCN)2PdCl2 DICHLOROBIS(ACETONITRILE)PALLADIUM(II) BIS(ACETONITRILE)PALLADIUM(II) CHLORIDE BIS(ACETONITRILE)PALLADIUM(II) DICHLORIDE bis(acetonitrile)dichloropalladium Palladium, bis(acetonitrile)dichloro- Di-(acetonitrile) palladium chloride chloranuidylpalladiobis(ylium)]chloranuide 14592-56-4 C4H6Cl2N2Pd C4H6N2PdCl2 C4Cl4N2Pd Catalysis and Inorganic Chemistry Homogeneous Pd Catalysts Transition Metal Compounds Homogeneous Catalysts