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BIS(3-AMINOPROPYL)PHENYLPHOSPHINE, with the molecular formula C15H25N2P, is a phosphine ligand characterized by a phenyl group and two amino propyl groups attached to a phosphorus atom. It is widely recognized for its effectiveness in metal-catalyzed reactions, such as cross-coupling and hydrogenation, and is instrumental in the preparation of organophosphorus compounds and the modification of polymers for diverse applications in materials science. Its versatility and capacity to enhance the reactivity of metal catalysts render it an invaluable asset in chemical research and industrial processes.

6775-01-5

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6775-01-5 Usage

Uses

Used in Organic Synthesis:
BIS(3-AMINOPROPYL)PHENYLPHOSPHINE is used as a phosphine ligand for enhancing the efficiency of various organic synthesis reactions. Its ability to stabilize metal catalysts and improve their reactivity contributes to the successful synthesis of complex organic molecules.
Used in Catalysis Reactions:
In the field of catalysis, BIS(3-AMINOPROPYL)PHENYLPHOSPHINE is used as a ligand to facilitate cross-coupling and hydrogenation reactions. Its presence in these reactions helps to achieve higher yields and selectivity, making it a preferred choice for chemists.
Used in the Preparation of Organophosphorus Compounds:
BIS(3-AMINOPROPYL)PHENYLPHOSPHINE is utilized as a key component in the synthesis of organophosphorus compounds, which are essential in various chemical and pharmaceutical applications.
Used in Materials Science:
In the realm of materials science, BIS(3-AMINOPROPYL)PHENYLPHOSPHINE is used for the modification of polymers, leading to the development of new materials with improved properties. Its role in polymer modification contributes to advancements in areas such as coatings, adhesives, and composite materials.
Used in Pharmaceutical Industry:
BIS(3-AMINOPROPYL)PHENYLPHOSPHINE is employed as a ligand in the synthesis of pharmaceutical compounds, where its ability to stabilize metal catalysts can lead to the production of more effective and selective drug molecules.
Used in Chemical Research:
In academic and industrial research settings, BIS(3-AMINOPROPYL)PHENYLPHOSPHINE is used as a versatile tool for exploring new reaction pathways and developing innovative synthetic methods, further expanding the scope of chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 6775-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,7 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6775-01:
(6*6)+(5*7)+(4*7)+(3*5)+(2*0)+(1*1)=115
115 % 10 = 5
So 6775-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H21N2P/c13-8-4-10-15(11-5-9-14)12-6-2-1-3-7-12/h1-3,6-7H,4-5,8-11,13-14H2/p+2

6775-01-5 Well-known Company Product Price

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  • Alfa Aesar

  • (10427)  Bis(3-aminopropyl)phenylphosphine   

  • 6775-01-5

  • 2g

  • 597.0CNY

  • Detail
  • Alfa Aesar

  • (10427)  Bis(3-aminopropyl)phenylphosphine   

  • 6775-01-5

  • 10g

  • 2980.0CNY

  • Detail
  • Alfa Aesar

  • (43675)  Bis(3-aminopropyl)phenylphosphine, packaged under Argon in resealable ChemSeal? bottles   

  • 6775-01-5

  • 2g

  • 1037.0CNY

  • Detail
  • Alfa Aesar

  • (43675)  Bis(3-aminopropyl)phenylphosphine, packaged under Argon in resealable ChemSeal? bottles   

  • 6775-01-5

  • 10g

  • 3771.0CNY

  • Detail

6775-01-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[3-aminopropyl(phenyl)phosphanyl]propan-1-amine

1.2 Other means of identification

Product number -
Other names Bis-<3-amino-propyl>-phenyl-phosphin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6775-01-5 SDS

6775-01-5Relevant academic research and scientific papers

Synthesis and investigation of phosphine ligands containing cationic guanidino functions in aqueous Heck reactions

Dibowski, Harald,Schmidtchen, Franz P.

, p. 2325 - 2330 (2007/10/02)

Phosphines 2 and 3 supplemented with strongly basic and hydrophilic guanidium functions were prepared for the first time. In combination with palladium acetate these ligands form active catalysts that promote an aqueous Heck reaction.

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