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TRI(2-FURYL)PHOSPHINE

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Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: +86-0371-55170693 +86-19937530512
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Products Intro: Product Name:Tri(2-furyl)phosphine
CAS:5518-52-5
Purity:99% Package:25KG;5KG;1KG
Company Name: Nanjing ChemLin Chemical Industry Co., Ltd.
Tel: 025-83697070
Email: product@chemlin.com.cn
Products Intro: CAS:5518-52-5
Purity:98% Package:g-Kg Remarks:White solid
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:Tri(2-furyl)phospine
CAS:5518-52-5
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
Company Name: career henan chemical co
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Products Intro: Product Name:TRI(2-FURYL)PHOSPHINE
CAS:5518-52-5
Purity:99% Package:1KG;1USD
Company Name: Accela ChemBio Inc.
Tel: +1-858-6993322
Email: info@accelachem.com
Products Intro: Product Name:Tri(2-furyl)phosphine
CAS:5518-52-5
Purity:>=98% Package:0.25g;1g;5g;10g;25g;100g;500g

TRI(2-FURYL)PHOSPHINE manufacturers

  • TRI(2-FURYL)PHOSPHINE
  • TRI(2-FURYL)PHOSPHINE pictures
  • $0.00 / 25kg
  • 2025-12-01
  • CAS:5518-52-5
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 10000KGS
TRI(2-FURYL)PHOSPHINE Basic information
Reaction
Product Name:TRI(2-FURYL)PHOSPHINE
Synonyms:SALOR-INT L308749-1EA;TRIS(2-FURYL)PHOSPHINE;TRI(2-FURYL)PHOSPHINE;Tri(2-furyl)phospine;Tri(2-furyl)phosphine,97%;Tri(2-furyL;TFP / Tri(2-furyl)phosphine;Tri(fur-2-yl)phosphine
CAS:5518-52-5
MF:C12H9O3P
MW:232.17
EINECS:628-036-8
Product Categories:Achiral Phosphine;Aryl Phosphine;organophosphorus ligand;Aromatics;Chelating Agents & Ligands;Heterocycles;Ligand;Phosphine Ligands;Synthetic Organic Chemistry;Catalysis and Inorganic Chemistry;Phosphine Ligands;Phosphorus Compounds
Mol File:5518-52-5.mol
TRI(2-FURYL)PHOSPHINE Structure
TRI(2-FURYL)PHOSPHINE Chemical Properties
Melting point 59-64 °C (lit.)
Boiling point 136 °C/4 mmHg (lit.)
Fp 136°C/4mm
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form solid
color faintly brown
Sensitive air sensitive
BRN 1577564
InChIInChI=1S/C12H9O3P/c1-4-10(13-7-1)16(11-5-2-8-14-11)12-6-3-9-15-12/h1-9H
InChIKeyDLQYXUGCCKQSRJ-UHFFFAOYSA-N
SMILESP(C1=CC=CO1)(C1=CC=CO1)C1=CC=CO1
CAS DataBase Reference5518-52-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-24/25
WGK Germany 3
10-23
TSCA No
HS Code 29319090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
TRI(2-FURYL)PHOSPHINE Usage And Synthesis
Reaction
  1. Useful ligand for C-C coupling reactions.
  2. Ligand used for the alkynylation of thioesters.
  3. Ligand used for enol ester formation.
  4. Ligand for palladium-catalyzed 3-Component coupling.
  5. Ligand for palladium-catalyzed C-C coupling reaction.
  6. Ligand for trans-olefin formation.
  7. Olefin formation from N-tosylhydrazones and benzyl halides.
  8. C-H arylation/alkenylation of 1-substituted tetrazoles. 
Reactions of 5518-52-5_1
Reactions of 5518-52-5_2
Chemical PropertiesTRI(2-FURYL)PHOSPHINE is white to light yellow crystal powde
UsesTRI(2-FURYL)PHOSPHINE is a phopshine ligand used in transition-metal mediated organic synthesis, in particular in wittig reactions to improved (Z) selectivity.
Usessuzuki reaction
reaction suitabilityreagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: ligand
reaction type: Cycloisomerizations
reagent type: ligand
reaction type: Heck Reaction
reagent type: ligand
reaction type: Negishi Coupling
reagent type: ligand
reaction type: Oxidations
reagent type: ligand
reaction type: Sonogashira Coupling
reagent type: ligand
reaction type: Stille Coupling
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling
Synthesis

The reaction flask was replaced with nitrogen atmosphere, under mechanical stirring, 20g of analytically pure furan, 34.8g of analytically pure TMEDA and 140mL of n-hexane were added into the reaction flask, 120mL of n-butyllithium (analytically pure) with a concentration of 2.5M/L was added dropwise at room temperature, after the dropwise addition was completed, the temperature was elevated to 50 and kept at 2h.

An analytically pure solution of 8g of n-hexane with a concentration of 3.5M/L of n-butyllithium (analytically pure) was added dropwise at 0 and kept at this temperature for 1h.

The reaction solution was poured into 200mL of saturated aqueous ammonium nitrate solution at 0, and stirred thoroughly, then the reaction solution was static stratified, and the organic phase was separated, and the aqueous phase was extracted with dichloromethane for 2-3 times, and the organic phase was combined, and the organic phase was concentrated to get the crude product, which was recrystallized with petroleum ether to get the crude product, and the crude product was extracted with petroleum ether to get the crude product, and the organic phase was concentrated to get the crude product. Recrystallized with petroleum ether, obtained white crystal product tris(2-furyl)phosphine 11.1g, the calculated yield was 82%, through the Agilent 1100 liquid chromatograph to get the product purity of 99.1%

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TRI(2-FURYL)PHOSPHINE Preparation Products And Raw materials
Preparation ProductsPhosphine oxide,tri-2-furanyl-
Tag:TRI(2-FURYL)PHOSPHINE(5518-52-5) Related Product Information
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