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S(-)-N,N-BIS(2-DIPHENYLPHOSPHINOETHYL)-1-PHENYLETHYLAMINE, also known as a chiral ligand, is a complex organic compound that plays a crucial role in the preparation of its iridium complexes. S(-)-N,N-BIS(2-DIPHENYLPHOSPHINOETHYL)-1-PHENYLETHYLAMINE is characterized by its unique structure, which allows it to form stable and efficient catalysts for various chemical reactions.

81510-19-2

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81510-19-2 Usage

Uses

Used in Pharmaceutical Industry:
S(-)-N,N-BIS(2-DIPHENYLPHOSPHINOETHYL)-1-PHENYLETHYLAMINE is used as a chiral ligand for the preparation of iridium complexes, which are essential in the synthesis of allylic alcohols. Allylic alcohols are valuable intermediates in the production of various pharmaceuticals, agrochemicals, and fine chemicals. The use of this chiral ligand in the synthesis process ensures the selective formation of desired enantiomers, which is crucial for the development of effective and safe drugs.
Used in Chemical Synthesis:
In the field of chemical synthesis, S(-)-N,N-BIS(2-DIPHENYLPHOSPHINOETHYL)-1-PHENYLETHYLAMINE is used as a chiral ligand for the preparation of iridium complexes. These complexes are employed as catalysts in the reduction of α,β-unsaturated ketones, a key step in the synthesis of various organic compounds. The use of this chiral ligand allows for the selective reduction of ketones, leading to the formation of specific enantiomers, which is essential for the development of enantioselective synthetic routes.
Used in Catalyst Development:
S(-)-N,N-BIS(2-DIPHENYLPHOSPHINOETHYL)-1-PHENYLETHYLAMINE is used as a chiral ligand in the development of new and improved catalysts for various chemical reactions. The unique structure of this ligand allows for the fine-tuning of catalyst properties, such as activity, selectivity, and stability. This enables chemists to design and synthesize catalysts that are tailored to specific applications, leading to more efficient and environmentally friendly processes.

Check Digit Verification of cas no

The CAS Registry Mumber 81510-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,1 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81510-19:
(7*8)+(6*1)+(5*5)+(4*1)+(3*0)+(2*1)+(1*9)=102
102 % 10 = 2
So 81510-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C36H37NP2/c1-31(32-17-7-2-8-18-32)37(27-29-38(33-19-9-3-10-20-33)34-21-11-4-12-22-34)28-30-39(35-23-13-5-14-24-35)36-25-15-6-16-26-36/h2-26,31H,27-30H2,1H3/t31-/m0/s1

81510-19-2 Well-known Company Product Price

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  • Aldrich

  • (14827)  (S)-(−)-N,N-Bis(2-diphenylphosphinoethyl)-1-phenylethylamine  ≥98.0% (CHN)

  • 81510-19-2

  • 14827-500MG

  • 2,667.60CNY

  • Detail

81510-19-2SDS

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 R-(+)-N,N-bis(2-diphenylphosphinoethyl)-1-phenylethylamine

1.2 Other means of identification

Product number -
Other names (R)-N,N-bis(2-diphenylphosphinoethyl)-1-phenyl-ethylamine

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:81510-19-2 SDS

81510-19-2Downstream Products

81510-19-2Relevant academic research and scientific papers

OPTISCH AKTIVE β(AMINO)ETHYL-PHOSPHONSAEUREESTER, β(AMINO)ETHYL-PHENYLPHOSPHINSAEUREESTER, β(AMINO)ETHYL-DIPHENYLPHOSPHINOXYDE UND β(AMINO)ETHYL-DIPHENYLPHOSPHINE

Maerkl, G.,Merkl, B.

, p. 4459 - 4462 (2007/10/02)

The title compounds are prepared by Michael-type additions of primary and secondary amines to P(O)-activated vinylsystems resp. diphenyl-vinylphosphine.

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