PCy3 Pd G2
95%
Manufacturer: Sigma Aldrich
CAS Number: 1353658-81-7
Synonym(S): Chloro[(tricyclohexylphosphine)-2-(2′-aminobiphenyl)]palladium(II), Tricyclohexylphosphine Pd G2
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 756741-1-G | In Stock | ₹ 11,100.00 |
| 5 G | 756741-5-G | In Stock | ₹ 30,147.60 |
756741 - 1 G
In Stock
Quantity
1
Base Price: ₹ 11,100.00
GST (18%): ₹ 1,998.00
Total Price: ₹ 13,098.00
Quality Level
100
Assay
95%
form
solid
feature
generation 2
reaction suitability
core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: C-H Activationreaction 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
244-246 °C
functional group
phosphine
SMILES string
NC1=C(C2=C([Pd]Cl)C=CC=C2)C=CC=C1.C3(CCCCC3)P(C4CCCCC4)C5CCCCC5
InChI
1S/C18H33P.C12H10N.ClH.Pd/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;/h16-18H,1-15H2;1-6,8-9H,13H2;1H;/q;;;+1/p-1
InChI key
CYJRABDADOSMKA-UHFFFAOYSA-M
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Sigma Aldrich Fine Chemicals Biosciences PCy3 Pd G2 95% | Purity: 95% | Mol Wt: 590.52 | 1353658-81-7 | MFCD21363051 | 1G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 12,053.69 | |
 | eMolecules Combi-Blocks Inc. Chloro[(tricyclohexylphosphine)-2-(2'-aminobiphenyl)]palladium(II) 5g 642135149 QH-3261 96.000 1353658-81-7 [null] 590.520 C30H43ClNPPd | eMolecules | ₹ 19,647.14 | |
| | Sigma Aldrich Fine Chemicals Biosciences PCy3 Pd G2 95% | Purity: 95% | Mol Wt: 590.52 | 1353658-81-7 | MFCD21363051 | 5G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 49,487.90 |
Description
- Application: PCy3 Pd G2 is a monophosphine-coordinated 2-phenylaniline-based palladacycle complex that can be used as a precatalyst:To prepare diarylmethanes by Suzuki cross-coupling reaction with heterocyclic-chloromethyl derivatives with aryl/heteroaryl boronic acids.[1] To synthesize poly(arylene)s by the Suzuki cross-coupling polymerization reaction between aryl dihalides and aryldiboronic acids.[2]In the C-H bond functionalization reactions.[3]
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Quality Level: 100
Assay: 95%
form: solid
feature: generation 2
reaction suitability: core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: C-H Activationreaction 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: 244-246 °C
functional group: phosphine
SMILES string: NC1=C(C2=C([Pd]Cl)C=CC=C2)C=CC=C1.C3(CCCCC3)P(C4CCCCC4)C5CCCCC5
InChI: 1S/C18H33P.C12H10N.ClH.Pd/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;/h16-18H,1-15H2;1-6,8-9H,13H2;1H;/q;;;+1/p-1
InChI key: CYJRABDADOSMKA-UHFFFAOYSA-M
Quality Level: 100
Assay: 97%
form: solid
feature: __
reaction suitability: __
mp: 183 °C (decomposition)
functional group: __
SMILES string: CC(=O)N1CN2CN(CP(C2)C1)C(C)=O
InChI: 1S/C9H16N3O2P/c1-8(13)11-3-10-4-12(9(2)14)7-15(5-10)6-11/h3-7H2,1-2H3
InChI key: MYJHMDGWZWBLCK-UHFFFAOYSA-N
Quality Level: 200
Assay: ≥99.0% (RT)
form: crystals
feature: __
reaction suitability: __
mp: 189.5 °C (dec.) (lit.)
functional group: __
SMILES string: __
InChI: __
InChI key: __