di-my-Chlorodimethylbis(triphenylphosphine)dipalladium
Product Information
Molecular Formula
C38H36Cl2P2Pd2
Molecular Weight
838.39
Description
di-my-Chlorodimethylbis(triphenylphosphine)dipalladium is a highly effective catalyst widely used in the biomedical industry. It plays a crucial role in various drug synthesis processes, particularly in the drug development of cancer and neurological disorders. This versatile compound assists in the development of novel drugs and therapeutic strategies, making it indispensable in the field of biomedicine.
Synonyms
carbanide; chloropalladium(1+); triphenylphosphane; Di-mu-chlorodimethylbis(triphenylphosphine)dipalladium 96per cent; Chloropalladium(1+) methanide--triphenylphosphane (1/1/1)
IUPAC Name
carbanidechloropalladium(1+)triphenylphosphane
SMILES
[CH3-].[CH3-].C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.Cl[Pd+].Cl[Pd+]
InChI
InChI=1S/2C18H15P.2CH3.2ClH.2Pd/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h2*1-15H2*1H32*1H/q2*-12*+2/p-2
InChI Key
XDSRKBHBQAZAOO-UHFFFAOYSA-L
Melting Point
216-220 °C
Flash Point
Not applicable
Purity
96%
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
6
Exact Mass
837.97430 g/mol
Monoisotopic Mass
835.97389 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
44
Formal Charge
0
Complexity
204
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
6
Compound Is Canonicalized
Yes
