Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct
Manufacturer: Sigma Aldrich
CAS Number: 52522-40-4
Synonym(S): Dipalladium-tris(dibenzylideneacetone)chloroform complex, Pd2(dba)3 · CHCl3
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 250 MG | 366315-250-MG | In Stock | ₹ 2,131.20 |
| 1 G | 366315-1-G | In Stock | ₹ 8,103.00 |
366315 - 250 MG
In Stock
Quantity
1
Base Price: ₹ 2,131.20
GST (18%): ₹ 383.616
Total Price: ₹ 2,514.816
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
131-135 °C (lit.)
SMILES string
[Pd].[Pd].ClC(Cl)Cl.O=C(/C=C/c1ccccc1)\C=C\c2ccccc2.O=C(/C=C/c3ccccc3)\C=C\c4ccccc4.O=C(\C=C\c5ccccc5)/C=C/c6ccccc6
InChI
1S/3C17H14O.CHCl3.2Pd/c3*18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16;2-1(3)4;;/h3*1-14H;1H;;/b3*13-11+,14-12+;;;
InChI key
LNAMMBFJMYMQTO-FNEBRGMMSA-N
Other Options
Related Products
Description
- General description: Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct (Pd2dba3·CHCl3) is reported to serve as effective precatalysts, or precursors to the active Pd(0) catalyst.[1]
- Application: Application Guide for Palladium Catalyzed Cross-Coupling Reactions
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P201 - P202 - P264 - P301 + P312 - P302 + P352 - P308 + P313
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Skin Irrit. 2
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
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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: 131-135 °C (lit.)
SMILES string: [Pd].[Pd].ClC(Cl)Cl.O=C(/C=C/c1ccccc1)\C=C\c2ccccc2.O=C(/C=C/c3ccccc3)\C=C\c4ccccc4.O=C(\C=C\c5ccccc5)/C=C/c6ccccc6
InChI: 1S/3C17H14O.CHCl3.2Pd/c3*18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16;2-1(3)4;;/h3*1-14H;1H;;/b3*13-11+,14-12+;;;
InChI key: LNAMMBFJMYMQTO-FNEBRGMMSA-N
form: liquid
Quality Level: 200
reaction suitability: core: tin
mp: −51 °C (lit.)
SMILES string: C[Sn](C)(C)c1ccccc1
InChI: 1S/C6H5.3CH3.Sn/c1-2-4-6-5-3-1;;;;/h1-5H;3*1H3;
InChI key: __
form: liquid
Quality Level: 200
reaction suitability: core: tin
mp: −51 °C (lit.)
SMILES string: C[Sn](C)(C)c1ccccc1
InChI: 1S/C6H5.3CH3.Sn/c1-2-4-6-5-3-1;;;;/h1-5H;3*1H3;
InChI key: __
