[1,3-Bis(diphenylphosphino)propane]palladium(II) triflate
Manufacturer: Sigma Aldrich
CAS Number: 137846-38-9
Synonym(S): Pd(OTf)2(dippp)
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 771384-1-G | In Stock | ₹ 22,655.10 |
771384 - 1 G
In Stock
Quantity
1
Base Price: ₹ 22,655.10
GST (18%): ₹ 4,077.918
Total Price: ₹ 26,733.018
form
solid
Quality Level
100
reaction suitability
core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Cross Couplingsreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalyst
mp
169-183 °C
SMILES string
[Pd++].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.C(CP(c1ccccc1)c2ccccc2)CP(c3ccccc3)c4ccccc4
InChI
1S/C27H26P2.2CHF3O3S.Pd/c1-5-14-24(15-6-1)28(25-16-7-2-8-17-25)22-13-23-29(26-18-9-3-10-19-26)27-20-11-4-12-21-27;2*2-1(3,4)8(5,6)7;/h1-12,14-21H,13,22-23H2;2*(H,5,6,7);/q;;;+2/p-2
InChI key
MIGUMLGJSGTNOK-UHFFFAOYSA-L
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | 137846-38-9 | Pd(OTf)2(dippp) | A2B Chem | -- |
Related Products
Description
- Application: [1,3-Bis(diphenylphosphino)propane]palladium(II) triflate can be used as a catalyst to synthesize phenanthridines by the reaction between 2-halogeno-N-Ms arylamines and benzyl halides/sulfonates via nucleophilic substitution followed by C-H functionalization and aromatization reaction.[1]
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P261 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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form: solid
Quality Level: 100
reaction suitability: core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Cross Couplingsreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalyst
mp: 169-183 °C
SMILES string: [Pd++].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.C(CP(c1ccccc1)c2ccccc2)CP(c3ccccc3)c4ccccc4
InChI: 1S/C27H26P2.2CHF3O3S.Pd/c1-5-14-24(15-6-1)28(25-16-7-2-8-17-25)22-13-23-29(26-18-9-3-10-19-26)27-20-11-4-12-21-27;2*2-1(3,4)8(5,6)7;/h1-12,14-21H,13,22-23H2;2*(H,5,6,7);/q;;;+2/p-2
InChI key: MIGUMLGJSGTNOK-UHFFFAOYSA-L
form: lyophilized powder
Quality Level: 100
reaction suitability: __
mp: __
SMILES string: __
InChI: __
InChI key: __
form: solid
Quality Level: 100
reaction suitability: reaction type: C-C Bond Formationreagent type: catalystreaction type: C-H Activation
mp: 151-157 °C
SMILES string: FC(F)(F)S(=O)O[Zn]OS(=O)C(F)(F)F
InChI: __
InChI key: __
