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Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) - 98% metals basis, high purity , CAS No.887919-35-9

COA

Grade & Purity:

≥98% metals basis

Cas Number: 887919-35-9
Molecular Weight: 708.07
MDL number: MFCD09265123
PubChem CID: 11714597
PubChem SID: 488197673

In stock

Item Number

B294172

Grouped product items
SKU	Size	Availability	Price
B294172-250mg	250mg	5	$153.90
B294172-1g	1g	2	$433.90
B294172-5g	5g	3	$1,533.90

Discover Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) by Aladdin Scientific in 98% metals basis for only $153.90. Available - in Ligands at Aladdin Scientific. Tags: .

Basic Description

Synonyms	887919-35-9 \| Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) \| Pd(amphos)Cl2 \| (A-taPhos)2PdCl2 \| PDCL2(AMPHOS)2 \| MFCD09265123 \| 4-ditert-butylphosphanyl-N,N-dimethylaniline;dichloropalladium \| bis(di-tert-butyl(4-dimethylaminophenyl)phosphine
Specifications & Purity	≥98% metals basis
Storage Temp	Argon charged
Shipped In	Normal
Product Description	Application Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) is a highly active, air-stable catalyst for Suzuki-Miyaura cross-coupling with aryl halides including 5- and 6-membered heteroaryl chlorides. A highly active, air-stable catalyst for Suzuki-Miyaura cross-coupling Product class M-P, Homogeneous Catalysts, Monodentate Ligands, Phosphorus Ligands - Achiral Reaction type Cross Coupling Reactions with Arenes, Suzuki-Miyaura Coupling Reaction Chemical properties Chemical formula C32H56N2Cl2P2Pd Empirical formula [Pd(amphos)2Cl2] Molecular weight 708.08 Metal Pd Theoretical metal content 15 Physical state powder Color yellow Metal purity 99.95 Applications & references Synthesis of the pyrazolopyridinone-based p38 mitogen-activated protein kinase inhibitor including a Suzuki coupling reaction. p38 MAP kinases are intercellular serine/threonine kinases which certainly regulate the production and action of several pro-inflammatory mediators. They are also involved in disease states such as rheumatoid arthritis, Crohn’s diseases and psoriasis. Reference: Org. Proc. Res. Dev. 2011, 15, 31. (DOI: 10.1021/op100205s)

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic nitrogen compounds
  - Class Organonitrogen compounds
    - Subclass Amines
      - Level5 Tertiary amines
        Level6 Tertiary alkylarylamines
        Level7 Dialkylarylamines

Kingdom	Organic compounds
Superclass	Organic nitrogen compounds
Class	Organonitrogen compounds
Subclass	Amines
Intermediate Tree Nodes	Tertiary amines - Tertiary alkylarylamines
Direct Parent	Dialkylarylamines
Alternative Parents	Aniline and substituted anilines Organic phosphines and derivatives Organic transition metal salts Hydrocarbon derivatives
Molecular Framework	Not available
Substituents	Aniline or substituted anilines - Dialkylarylamine - Benzenoid - Monocyclic benzene moiety - Phosphine - Organic metal salt - Organic transition metal salt - Hydrocarbon derivative - Organophosphorus compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as dialkylarylamines. These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	488197673
IUPAC Name	4-ditert-butylphosphanyl-N,N-dimethylaniline;dichloropalladium
INCHI	InChI=1S/2C16H28NP.2ClH.Pd/c21-15(2,3)18(16(4,5)6)14-11-9-13(10-12-14)17(7)8;;;/h29-12H,1-8H3;2*1H;/q;;;;+2/p-2
InChIKey	DWOZNANUEDYIOF-UHFFFAOYSA-L
Smiles	CC(C)(C)P(C1=CC=C(C=C1)N(C)C)C(C)(C)C.CC(C)(C)P(C1=CC=C(C=C1)N(C)C)C(C)(C)C.Cl[Pd]Cl
Isomeric SMILES	CC(C)(C)P(C1=CC=C(C=C1)N(C)C)C(C)(C)C.CC(C)(C)P(C1=CC=C(C=C1)N(C)C)C(C)(C)C.Cl[Pd]Cl
WGK Germany	3
PubChem CID	11714597
Molecular Weight	708.07

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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5 results found

Lot Number	Certificate Type	Date	Item
C2526107	Certificate of Analysis	Apr 12, 2025	B294172
A2331048	Certificate of Analysis	Nov 11, 2024	B294172
A2331047	Certificate of Analysis	Nov 07, 2024	B294172
A23301209	Certificate of Analysis	Nov 07, 2024	B294172
A23301205	Certificate of Analysis	Nov 07, 2024	B294172

Chemical and Physical Properties

Molecular Weight	708.100 g/mol
XLogP3
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	8
Exact Mass	706.233 Da
Monoisotopic Mass	706.233 Da
Topological Polar Surface Area	6.500 Å²
Heavy Atom Count	39
Formal Charge	0
Complexity	240.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	3

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