Diphenyl(p-tolyl)phosphine
96%
Manufacturer: Sigma Aldrich
CAS Number: 1031-93-2
Synonym(S): (4-Methylphenyl)diphenyl phosphine
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 10 G | 155039-10-G | In Stock | ₹ 2,641.30 |
155039 - 10 G
In Stock
Quantity
1
Base Price: ₹ 2,641.30
GST (18%): ₹ 475.434
Total Price: ₹ 3,116.734
Quality Level
100
Assay
96%
form
liquid
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
66-68 °C (lit.)
functional group
phosphine
SMILES string
Cc1ccc(cc1)P(c2ccccc2)c3ccccc3
InChI
1S/C19H17P/c1-16-12-14-19(15-13-16)20(17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-15H,1H3
InChI key
QJIMTLTYXBDJFC-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | eMolecules DIPHENYL(P-TOLYL)PHOSPHINE | 1031-93-2 | MFCD00008543 | 100G | eMolecules | -- | |
 | Diphenyl(p-tolyl)phosphine | ChemScene | ₹ 4,717.00 - ₹ 46,102.00 | |
 | 1031-93-2 | Diphenyl(p-tolyl)phosphine | A2B Chem | ₹ 801.00 - ₹ 13,973.00 |
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Description
- Application: Reactant for:Three-component cyclizationProbing coordination ability via a palladium pincer complexChelation-assisted hydroacylation of olefins with primary alcoholsReactant for synthesis of:Trinuclear ruthenium carbonyl triarylphosphine cluster complexesLeishmanicidal leads targeting mitochondria through inhibition of the respiratory complexInP nanofibers / metal phosphide nanostructuresPeroxyl radical cations via pulse radiolysis one-electron oxidations
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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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Quality Level: 100
Assay: 96%
form: liquid
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: 66-68 °C (lit.)
functional group: phosphine
SMILES string: Cc1ccc(cc1)P(c2ccccc2)c3ccccc3
InChI: 1S/C19H17P/c1-16-12-14-19(15-13-16)20(17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-15H,1H3
InChI key: QJIMTLTYXBDJFC-UHFFFAOYSA-N
Quality Level: 100
Assay: __
form: powder
reaction suitability: reaction type: Boc solid-phase peptide synthesis
mp: ~90 °C (dec.)
functional group: __
SMILES string: Cc1ccc(cc1)S(=O)(=O)NC(=N)NCCC[C@H](NC(=O)OC(C)(C)C)C(O)=O
InChI: 1S/C18H28N4O6S/c1-12-7-9-13(10-8-12)29(26,27)22-16(19)20-11-5-6-14(15(23)24)21-17(25)28-18(2,3)4/h7-10,14H,5-6,11H2,1-4H3,(H,21,25)(H,23,24)(H3,19,20,22)/t14-/m0/s1
InChI key: WBIIPXYJAMICNU-AWEZNQCLSA-N
Quality Level: 100
Assay: 95%
form: liquid
reaction suitability: __
mp: __
functional group: __
SMILES string: C[Si](C)(C)N=[N+]=[N-]
InChI: 1S/C3H9N3Si/c1-7(2,3)6-5-4/h1-3H3
InChI key: SEDZOYHHAIAQIW-UHFFFAOYSA-N
