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1,1-bis(diphenyphosphino)ferrocene

1,1-bis(diphenyphosphino)ferrocene

CAS: 12150-46-8

Molecular Formula: C34H28FeP2

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1,1-bis(diphenyphosphino)ferrocene - Names and Identifiers

Name 1,1-bis(diphenyphosphino)ferrocene
Synonyms DPPF
iron
1,1-bis(diphenyphosphino)ferrocene
1,1-Ferrocenebis(diphenylphosphine)
1,1-Bis(diphenylphosphino)ferrocene
1,1-Ferrocenediyl-bis(diphenylphosphine)
1-cyclopenta-2,4-dienyl-diphenyl-phosphane
bis(2-diphenylphosphanylcyclopenta-2,4-dien-1-yl)iron
CAS 12150-46-8
EINECS 430-420-3
InChI InChI=1/2C17H14P.Fe/c2*1-3-9-15(10-4-1)18(17-13-7-8-14-17)16-11-5-2-6-12-16;/h2*1-14H;/rC34H28FeP2/c1-5-15-27(16-6-1)36(28-17-7-2-8-18-28)33-25-13-23-31(33)35-32-24-14-26-34(32)37(29-19-9-3-10-20-29)30-21-11-4-12-22-30/h1-26,31-32H

1,1-bis(diphenyphosphino)ferrocene - Physico-chemical Properties

Molecular FormulaC34H28FeP2
Molar Mass554.379
Melting Point181-183℃
Water SolubilitySoluble in chloroform, dichloromethane, alcohol and pentane. Insoluble in water. 7: reacts slowly with moisture/water
Appearanceyellow to orange crystal
Storage Condition2-8°C
StabilityStable. Incompatible with strong oxidizing agents. Air Sensitive
Physical and Chemical PropertiesMelting point 181-183°C.
UseA ligand for the synthesis of oxazepine ring system in a palladium-catalyzed coupling reaction; Preparation of novel functionalized furan derivatives by continuous C- C and C- O bonding reactions of palladium phosphonates; Transition metal complexes, an effective catalyst for cross-coupling reactions of Grignard reagents with organic halides and related compounds; A diphosphine ligand, complexes with transition metals can be used as C- C/C-N/C-O coupling reactions and other organic synthesis catalysts

1,1-bis(diphenyphosphino)ferrocene - Risk and Safety

Hazard SymbolsT - Toxic
Toxic
Risk CodesR25 - Toxic if swallowed
Safety DescriptionS45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDs3467
WGK Germany3
FLUKA BRAND F CODES10-23
TSCANo
HS Code29319090
Hazard ClassIRRITANT

1,1-bis(diphenyphosphino)ferrocene - Upstream Downstream Industry

Raw MaterialsSodium hydroxide
Ethyl acetate
Tetrahydrofuran
Dichloromethane
n-Butyllithium
N,N,N',N'-Tetramethylethylenediamine
Ferrocene
Dicyclopentadiene
Ferrous chloride
Chlorodiphenylphosphine
Lithium, [1-(diphenylphosphino)-2,4-cyclopentadien-1-yl]-
Diphenylphosphinoferrocene
1,1'-bis(diphenylphosphinyl)-Ferrocene
4,4'-Bis(t-butyl)-1,1',2,2'-tetrakis(diphenylphosphino)ferrocene, 98% HiersoPHOS-5
DIMETHYLPHENYLPHOSPHINE
Sodium thiocyanate
Sodium diethyldithiocarbamate
Phenyllithium
Downstream Products[1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)
N,N'-Bis- (1-naphthalenyl)-N,N'-bis-phenyl-(1,1'-biphenyl)-4,4'-diamine
1,1'-Bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex
[1,1'-Bis(diphenylphosphino)ferrocene]dichloronickel(II)

1,1-bis(diphenyphosphino)ferrocene - Introduction

Melting point 181-182°C (dec.)(lit.)

Storage conditions 2-8°C

morphological crystal

color yellow to orange

water solubility Soluble in chloroform, dichloromethane, alcohol and pentane. Insoluble in water.

hydrolysis sensitivity 7: reacts slowly with moisture/water

Sensitivity Air Sensitive

stability stable. Incompatible with strong oxidizing agents.

application

1,1 '-bis (diphenylphosphine) ferrocene is used to synthesize ligands of oxazepine ring system in palladium-catalyzed coupling reaction; novel functionalized furan derivatives are prepared by continuous C- C of palladium phosphinate and C- O bonding reaction; transition metal complex, an effective catalyst for cross-coupling reaction between Gliya reagent (Grignardreagents) and organic halides and related compounds.

Uses Used for the synthesis of ligands of oxazepine ring systems in palladium-catalyzed coupling reactions; preparation of novel functionalized furan derivatives through continuous C- C of palladium phosphinates and C- O bonding reactions; transition metal complexes, Used as an effective catalyst for the cross-coupling reaction of Gliya reagents (Grignard reagents) with organic halides and related compounds; a diphosphine ligand, complexes with transition metals can be used as organic synthesis catalysts such as C- C/C-N/C-O coupling reactions

Use organometallic catalyst (ligand). New functionalized furan derivatives were prepared by palladium-phosphine catalyzed C- C and C- O bond sequential bonding reaction.

safety information

dangerous goods mark T,Xi,Xn

Hazard category code 25-36/37/38-20/21/22

Safety instructions 22-24/25-45-28A-36-26-36/37/39

Dangerous Goods Transport No. 3467

WGK Germany 3

F 10-23

TSCA No

HazardClass IRRITANT

customs code 29319090

Last Update:2024-04-10 22:29:15
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View History
1,1-bis(diphenyphosphino)ferrocene
1-(2,6-Dichloro-3-fluorophenyl)ethanol
季戊四醇四(2-氰基-3,3-二苯丙烯酸酯)
5-Decen-1-ol, (5Z)-
Raw Materials for 1,1-bis(diphenyphosphino)ferrocene
Sodium hydroxide
Ethyl acetate
n-Butyllithium
N,N,N',N'-Tetramethylethylenediamine
Ferrocene
Chlorodiphenylphosphine
Phenyllithium
Downstream Products for 1,1-bis(diphenyphosphino)ferrocene
[1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)
N,N'-Bis- (1-naphthalenyl)-N,N'-bis-phenyl-(1,1'-biphenyl)-4,4'-diamine
1,1'-Bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex
[1,1'-Bis(diphenylphosphino)ferrocene]dichloronickel(II)
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