dichlorobis(di-tert-butylphenylphosphine)palladium(II)
Product Information
Molecular Formula
C28H46Cl2P2Pd
Molecular Weight
621.95
Description
Effective catalyst for cross-coupling reactions.
Synonyms
ditert-butyl(phenyl)phosphane; dichloropalladium; Dichlorobis(di-tert-butylphenylphosphine) palladium(II); Dichlorobis(di-t-butylphenylphosphino)palladium(II), 99%; Dichlorobis(di-t-butylphenylphosphino)palladium(II); Y-200033; bis(di-t-butyl phenyl phosphine) palladium dichloride; Dichlorobis(di-tert-butylphenylphosphine)palladium(II), 95%
IUPAC Name
ditert-butyl(phenyl)phosphanedichloropalladium
SMILES
CC(C)(C)P(C1=CC=CC=C1)C(C)(C)C.CC(C)(C)P(C1=CC=CC=C1)C(C)(C)C.Cl[Pd]Cl
InChI
InChI=1S/2C14H23P.2ClH.Pd/c2*1-13(2,3)15(14(4,5)6)12-10-8-7-9-11-12/h2*7-11H,1-6H32*1H/q+2/p-2
InChI Key
QNNRAWADYXIGHE-UHFFFAOYSA-L
Melting Point
260-264 °C (decomposition)
Flash Point
Not applicable
Purity
95%
Safety Information
Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
6
Exact Mass
620.14866 g/mol
Monoisotopic Mass
620.14866 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
33
Formal Charge
0
Complexity
177
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
3
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| WO-2021062035-A1 | Luminescent materials and methods thereof | 2019-09-27 |
| WO-2019214084-A1 | Method for biocatalytic synthesis of sitagliptin and intermediate thereof | 2018-05-10 |
| US-2021123080-A1 | Method for biocatalytic synthesis of sitagliptin and intermediate thereof | 2018-05-10 |
| EP-3583093-B1 | Process for preparing substituted biphenyls | 2017-02-14 |
| ES-2880323-T3 | Process for the preparation of substituted biphenyls | 2017-02-14 |
| US-2020039914-A1 | Cyclohexyl gpr40 agonists for the treatment of type ii diabetes | 2016-10-25 |
| US-10988433-B2 | Cyclohexyl GPR40 agonists for the treatment of type II diabetes | 2016-10-25 |
| US-10106553-B2 | Substituted benzothiophenyl derivatives as GPR40 agonists for the treatment of type II diabetes | 2016-04-11 |
| US-10195178-B2 | GPR40 agonists in anti-diabetic drug combinations | 2016-04-11 |
| US-2017290800-A1 | Gpr40 agonists in anti-diabetic drug combinations | 2016-04-11 |
