(1,3-Bis(diphenylphosphino)propane)palladium(II) chloride
Product Information
Molecular Formula
C27H26Cl2P2Pd
Molecular Weight
589.77
Description
(1,3-Bis(diphenylphosphino)propane)palladium(II) chloride enjoys a prominent role as a ubiquitous catalyst precursor. In particular, pharmaceutical realms deeply appreciate its efficacy, with employments mainly featuring cross-coupling reactions.
Synonyms
Dichloro[1,3-bis(diphenylphosphino)propane]palladium(II), PdCl2(dippp)
IUPAC Name
dichloropalladium3-diphenylphosphanylpropyl(diphenyl)phosphane
SMILES
C1=CC=C(C=C1)P(CCCP(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4.Cl[Pd]Cl
InChI
InChI=1S/C27H26P2.2ClH.Pd/c1-5-14-24(15-6-1)28(25-16-7-2-8-17-25)22-13-23-29(26-18-9-3-10-19-26)27-20-11-4-12-21-27/h1-12,14-21H,13,22-23H22*1H/q+2/p-2
InChI Key
LDFBXJODFADZBN-UHFFFAOYSA-L
Boiling Point
529.7°C at 760 mmHg
Flash Point
Not applicable
Purity
95%
Safety Information
Hazards
H302 + H312 + H332 - H315 - H319 - H335
Precautionary Statement
P280 - P301 + P312 + P330 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
8
Exact Mass
587.99216 g/mol
Monoisotopic Mass
587.99216 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
32
Formal Charge
0
Complexity
353
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
2
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113845544-A | Preparation method of organometallic compound [1, 3-bis (diphenylphosphino) propane ] palladium (II) chloride | 2021-10-29 |
| CN-112174995-A | Double-silicon compound, preparation method and application thereof | 2020-10-27 |
| CN-112174995-B | Double-silicon compound, preparation method and application thereof | 2020-10-27 |
| KR-102345758-B1 | Palladium single-atom catalyst supported on C@C3N4 for electrochemical reactions and method for preparing the same | 2020-06-24 |
| JP-2021187753-A | Method for producing 2,3,4,5,6-pentafluorostyrene | 2020-05-27 |
| EP-3909950-A1 | Heterocyclic compounds for the control of invertebrate pests | 2020-05-13 |
| CN-111303151-A | Aza, oxa, mixed nitrogen/oxa-hydrogenated annulated [ n ] arenes and preparation method thereof | 2020-03-04 |
| WO-2021117767-A1 | Method for producing nitrogen-containing heteroarylcarboxamide acetic acid derivative | 2019-12-10 |
| WO-2021062035-A1 | Luminescent materials and methods thereof | 2019-09-27 |
| WO-2021024675-A1 | Compound and production method therefor | 2019-08-05 |
