BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)

Product Name: BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)
CAS No.: 251567-28-9
Chemical Name: BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)
Synonyms: [Pd(NCOC2H4CO)(PPh3)2Br];BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II);bromo(n-succinimidyl)bis(triphenylphosphine)palladium(ii);trans-Bromo(N-succinimidyl)bis(triphenylphosphine)palladium(II);bromopalladium, pyrrolidin-1-ide-2,5-dione, triphenylphospho...;trans-BroMo(N-succiniMidyl)bis(triphenylphosphine)palladiuM(II),97%;BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)
CBNumber: CB5972889
Molecular Formula: C40H37BrNO2P2Pd
Formula Weight: 812.01
MOL File: 251567-28-9.mol

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BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Property

Melting point:: 223-228 °C (dec.) (lit.)
form: solid

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Safety

WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 643742
Product name: trans-Bromo(N-succinimidyl)bis(triphenylphosphine)palladium(II)
Purity: 97%
Packaging: 1g
Price: $236
Updated: 2022/05/15

American Custom Chemicals Corporation

Product number: OGM0000683
Product name: TRANS-BROMO(N-SUCCINIMIDYL)BIS(TRIPHENYLPHOSPHINE)PALLADIUM(II)
Purity: 95.00%
Packaging: 1G
Price: $790.1
Updated: 2021/12/16

Arctom

Product number: AS289080
Product name: Trans-Bromo(N-succinimidyl)bis(triphenylphosphine)palladium(II)
Purity: 98%
Packaging: 1g
Price: $371
Updated: 2021/12/16

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BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Chemical Properties,Usage,Production

Uses

trans-Bromo(N-succinimidyl)bis(triphenylphosphine)palladium(II) may be used in the following processes:

As a catalyst for the preparation of 6-cyano-2-(3-fluoro-benzyl)-indole-1-carboxylic acid tert-butyl ester via Suzuki cross-coupling reaction between 1-boc-6-cyanoindole-2-boronic acid and 3-fluorobenzyl bromide. This method does not involve the use of strong bases or toxic reagents and also the use of this catalyst minimizes protodeboronation.
As a precatalyst for the Suzuki-Miyaura cross-coupling reaction between alkenyl tosylates and alkenyl MIDA boronates in the absence of phosphine ligands. For less activated alkenyl tosylate, the addition of tricyclohexylphosphine tetrafluoroborate improves the reactivity.

reaction suitability

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst

BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Preparation Products And Raw materials

Raw materials

Preparation Products

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BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Suppliers

China 19 South Korea 1 Switzerland 1 United States 2 Global 23

Energy Chemical

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Sigma-Aldrich

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251567-28-9, BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)Related Search:

Succinimide

[Pd(NCOC2H4CO)(PPh3)2Br]

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bromo(n-succinimidyl)bis(triphenylphosphine)palladium(ii)

trans-Bromo(N-succinimidyl)bis(triphenylphosphine)palladium(II)

trans-BroMo(N-succiniMidyl)bis(triphenylphosphine)palladiuM(II),97%

bromopalladium, pyrrolidin-1-ide-2,5-dione, triphenylphospho...

BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)

251567-28-9

C40H34BrNO2P2Pd