Structure of Bistert butyldicylcohexylphosphinedichloropalladiumII CAS 104889 13 6 554x400 - Bis(tert-butyldicylcohexylphosphine)dichloropalladium(II) CAS 104889-13-6

Iden­ti­fi­ca­tion

CAS Number

104889-13-6

Name

Bis(tert-butyldicylcohexylphosphine)dichloropalladium(II)

Syn­onyms

Dichlorobis[(tert-butyl)dicyclohexylphosphine]palladium(II);
bis(tert-butyldicyclohexyl-l5-phosphaneyl)palladium(IV)chlo­ride ;
CX82

Std­InChIKey

OMJWQFN­HIXGKJO-UHF­F­­FAOYSA-L

Mol­e­c­u­lar Formula

C32H62P2Cl2Pd

Mol­e­c­u­lar Weight

686.11

Prop­er­ties

Appear­ance

Yel­low to orange crys­talline powder

Safe­ty Data

RIDADR 

NONH for all modes of transport

WGK Germany

3

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our Bis(tert-butyldicylcohexylphosphine)dichloropalladium(II) CAS 104889-13-6

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

98% min

Shelf Life

2 years

Stor­age

Do not store above 25°C (77°F). Store in a tight­ly closed orig­i­nal con­tain­er, pro­tect­ed from direct sun­light in a dry, cool and well-ven­ti­lat­ed area.

Known Appli­ca­tion

  1. High-effi­­cien­­cy Suzu­ki cou­pling reac­tion cat­a­lyst, for the cou­pling of aryl boron­ic acid and aryl chlo­ride, the yield of more than 90% can be achieved with a feed­ing amount of 0.01~0.1%
  2. For the cou­pling of aryl boron­ic acid and aryl bro­mide, the yield of 0.005% to 0.01% of the feed­ing amount can achieve a yield of more than 95%
  3. It also has good cat­alyt­ic con­ver­sion effect for C-N coupling
  4. The cou­pling reac­tion of two-phase or even mul­ti-phase sys­tems such as water/​ethanol, water/​toluene, water/​tetrahydrofuran can be realized
  5. Spe­cial activ­i­ty for dif­­fi­cult-to-react cou­pling reac­tions with large steric hin­drance or insuf­fi­cient func­tion­al group activity

This prod­uct is devel­oped by our R&D com­pa­ny Warshel Chem­i­cal Ltd (https://​www​.warshel​.com/).

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