741825
XPhos Pd G2
98%, solid
Synonym(s):
2nd Generation XPhos Precatalyst, Chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II), X-Phos aminobiphenyl palladium chloride precatalyst, XPhos-Pd-G2
Select a Size
| Size/SKU | Availability | Price |
|---|---|---|
250 mg | Estimated to ship onSeptember 08, 2026fromMILWAUKEE | $49.60 |
1 g | Estimated to ship onSeptember 08, 2026fromMILWAUKEE | $156.00 |
5 g | Estimated to ship onSeptember 08, 2026fromMILWAUKEE | $557.00 |
10 g | Estimated to ship onSeptember 08, 2026fromMILWAUKEE | $1,070.00 |
25 g | Estimated to ship onSeptember 08, 2026fromMILWAUKEE | $2,070.00 |
100 g | Estimated to ship onSeptember 08, 2026fromMILWAUKEE | $6,740.00 |
500 g | Estimated to ship onSeptember 08, 2026fromMILWAUKEE | $18,940.00 |
About This Item
$49.60
Estimated to ship onSeptember 08, 2026Details
Product Name
XPhos Pd G2, 98%
Quality Segment
product line
Buchwald precatalyst Generation 2
assay
98%
form
solid
feature
generation 2
reaction suitability
core: palladium, reaction type: Buchwald-Hartwig Cross Coupling Reaction, 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
reaction type: Cross Couplings
mp
202-210 °C
functional group
phosphine
SMILES string
Nc1ccccc1-c2ccccc2[Pd]Cl.Nc3ccccc3-c4ccccc4[Pd]Cl.CC(C)c5cc(C(C)C)c(-c6cccc(c6)P(C7CCCCC7)C8CCCCC8)c(c5)C(C)C.CC(C)c9cc(C(C)C)c(c(c9)C(C)C)-c%10ccccc%10P(C%11CCCCC%11)C%12CCCCC%12
InChI
1S/2C33H49P.2C12H10N.2ClH.2Pd/c1-23(2)27-21-31(24(3)4)33(32(22-27)25(5)6)26-14-13-19-30(20-26)34(28-15-9-7-10-16-28)29-17-11-8-12-18-29;1-23(2)26-21-30(24(3)4)33(31(22-26)25(5)6)29-19-13-14-20-32(29)34(27-15-9-7-10-16-27)28-17-11-8-12-18-28;2*13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;;;/h13-14,19-25,28-29H,7-12,15-18H2,1-6H3;13-14,19-25,27-28H,7-12,15-18H2,1-6H3;2*1-6,8-9H,13H2;2*1H;;/q;;;;;;2*+1/p-2
InChI key
HMRJFNBZAWHTGN-UHFFFAOYSA-L
General description
Application
- Palladium-catalyzed Suzuki-Miyaura coupling reactions of potassium organotrifluoroborates and sulfamates.
- Suzuki-Miyaura cross-coupling reactions of sensitive aryl and heteroarylboronic acids.
- Synthesis of potassium Boc-protected secondary aminomethyltrifluoroborates, via Suzuki-Miyaura cross-coupling reaction.
1 of 1
This Item | |||
|---|---|---|---|
| description 98% | description 98%, 1:1 MTBE adduct | description - | description 95% |
| reaction suitability reaction type: Sonogashira Coupling, reaction type: Heck Reaction, reaction type: Negishi Coupling, reaction type: Suzuki-Miyaura Coupling, core: palladium, reaction type: Stille Coupling, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reagent type: catalyst | reaction suitability core: palladium, reaction type: Heck Reaction, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reagent type: catalyst | reaction suitability core: palladium, reaction type: Sonogashira Coupling, reaction type: Suzuki-Miyaura Coupling, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reagent type: catalyst | reaction suitability reaction type: Hiyama Coupling, reaction type: Heck Reaction, reaction type: Sonogashira Coupling, reagent type: catalyst |
| assay 98% | assay 98% | assay - | assay 95% |
| form solid | form solid | form solid | form solid |
| functional group phosphine | functional group phosphine | functional group phosphine | functional group phosphine |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| mp 202-210 °C | mp 146-151 °C (decomposition) | mp 218 °C (dec.) | mp 152-163 °C (decomposition) |
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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