cataCXium® A Pd G2
Manufacturer: Sigma Aldrich
CAS Number: 1375477-29-4
Synonym(S): cataCXium A-Pd-G2, Chloro[(di(1-adamantyl)-N-butylphosphine)-2-(2-aminobiphenyl)]palladium(II)
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 250 MG | 761311-250-MG | In Stock | ₹ 5,816.40 |
| 1 G | 761311-1-G | In Stock | ₹ 21,101.10 |
| 5 G | 761311-5-G | In Stock | ₹ 74,303.40 |
761311 - 250 MG
In Stock
Quantity
1
Base Price: ₹ 5,816.40
GST (18%): ₹ 1,046.952
Total Price: ₹ 6,863.352
form
solid
Quality Level
100
feature
generation 2
reaction suitability
reaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalystreaction type: Cross Couplings
mp
220 °C (decomposition)
functional group
aminephosphine
SMILES string
Nc1ccccc1-c2ccccc2[Pd]Cl.CCCCP([C@@]34C[C@@H]5C[C@@H](C[C@@H](C5)C3)C4)[C@@]67C[C@@H]8C[C@@H](C[C@@H](C8)C6)C7
InChI
1S/C24H39P.C12H10N.ClH.Pd/c1-2-3-4-25(23-11-17-5-18(12-23)7-19(6-17)13-23)24-14-20-8-21(15-24)10-22(9-20)16-24;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;/h17-22H,2-16H2,1H3;1-6,8-9H,13H2;1H;/q;;;+1/p-1/t17-,18+,19-,20-,21+,22-,23-,24-;;;
InChI key
CAVPLNLGXHYGIR-DVBMAMJVSA-M
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Sigma Aldrich Fine Chemicals Biosciences cataCXium(R) A Pd G2 | 1375477-29-4 | MFCD22200549 | 250MG | Sigma Aldrich Fine Chemicals Biosciences | ₹ 9,485.18 | |
 | Sigma Aldrich Fine Chemicals Biosciences cataCXium(R) A Pd G2 | 1375477-29-4 | MFCD22200549 | 5G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 93,085.86 | |
 | 1375477-29-4 | Chloro[(di(1-adamantyl)-n-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) | A2B Chem | ₹ 427.80 - ₹ 36,106.32 |
Related Products
Description
- Application: cataCXium® A Pd G2 is a Buchwald′s second generation catalyst that can be used as a palladium source for the coupling of potassium 1-(benzyloxy)alkyltrifluoroborates with aryl and heteroaryl chlorides via Suzuki-Miyaura reaction to yield protected secondary alcohols.[1]
- Legal Information: cataCXium is a registered trademark of Umicore AG & Co. KG
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Show Difference
form: solid
Quality Level: 100
feature: generation 2
reaction suitability: reaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalystreaction type: Cross Couplings
mp: 220 °C (decomposition)
functional group: aminephosphine
SMILES string: Nc1ccccc1-c2ccccc2[Pd]Cl.CCCCP([C@@]34C[C@@H]5C[C@@H](C[C@@H](C5)C3)C4)[C@@]67C[C@@H]8C[C@@H](C[C@@H](C8)C6)C7
InChI: 1S/C24H39P.C12H10N.ClH.Pd/c1-2-3-4-25(23-11-17-5-18(12-23)7-19(6-17)13-23)24-14-20-8-21(15-24)10-22(9-20)16-24;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;/h17-22H,2-16H2,1H3;1-6,8-9H,13H2;1H;/q;;;+1/p-1/t17-,18+,19-,20-,21+,22-,23-,24-;;;
InChI key: CAVPLNLGXHYGIR-DVBMAMJVSA-M
form: __
Quality Level: 300
feature: __
reaction suitability: __
mp: 67-72 °C (lit.)
functional group: __
SMILES string: __
InChI: __
InChI key: __
form: solid
Quality Level: 100
feature: __
reaction suitability: reaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: ligand
mp: >300 °C
functional group: phosphine
SMILES string: __
InChI: 1S/C48H52O4P2/c1-29-13-30(2)18-39(17-29)53(40-19-31(3)14-32(4)20-40)45-27-37(49-9)25-43(51-11)47(45)48-44(52-12)26-38(50-10)28-46(48)54(41-21-33(5)15-34(6)22-41)42-23-35(7)16-36(8)24-42/h13-28H,1-12H3
InChI key: IDNKFBDRZBLTFQ-UHFFFAOYSA-N
