341968-71-6 Usage
Uses
Used in Organic Synthesis:
(1S,2S)-2-Amino-1-phenylpropyldiphenylphosphine, min. 97% is used as a ligand in catalytic reactions, particularly in asymmetric catalysis. Its unique structure and chirality make it a valuable reagent for the synthesis of enantioselective compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1S,2S)-2-Amino-1-phenylpropyldiphenylphosphine, min. 97% is utilized in the development and production of fine chemicals and active pharmaceutical ingredients. Its ability to act as a ligand in catalytic reactions aids in the synthesis of complex molecules with specific stereochemistry, which is crucial for the efficacy and safety of many drugs.
Used in Production of Fine Chemicals:
(1S,2S)-2-Amino-1-phenylpropyldiphenylphosphine, min. 97% is also employed in the production of fine chemicals, where its chiral properties and catalytic capabilities contribute to the creation of high-quality specialty chemicals for various applications, including fragrances, dyes, and other performance chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 341968-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,1,9,6 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 341968-71:
(8*3)+(7*4)+(6*1)+(5*9)+(4*6)+(3*8)+(2*7)+(1*1)=166
166 % 10 = 6
So 341968-71-6 is a valid CAS Registry Number.
341968-71-6Relevant academic research and scientific papers
Synthesis of chiral aminophosphines from chiral aminoalcohols via cyclic sulfamidates
Guo, Rongwei,Lu, Shuiming,Chen, Xuanhua,Tsang, Chi-Wing,Jia, Wenli,Sui-Seng, Christine,Amoroso, Dino,Abdur-Rashid, Kamaluddin
supporting information; experimental part, p. 937 - 940 (2010/05/02)
(Chemical Equation Presented) Protic aminophosphines with multiple chiral centers were synthesized in good yields and high purity by the nucleophilic ring-opening of N-protected cyclic sulfamidates with metal phosphides, followed by hydrolysis and deprote
METHOD FOR THE PREPARATION OF AMINOPHOSPHINE LIGANDS AND THEIR USE IN METAL CATALYSTS
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Page/Page column 41-42, (2009/01/24)
The present application is directed to i) a two-step method for synthesizing phosphme-ammophosphme (P,N,P) ligands, ii) the use of such ligands in the preparation of metal complexes as hydrogenation catalysts, and iii) ammophosphme (P,N) and phosphme-ammo
Funktionelle Phosphane: Part XI. Optisch reine β-Aminophosphane und β-Aminophosphinite für die komplexkatalysierte Reduktion organischer Carbonylverbindungen. Molekülstrukturen von [(1R,2R)-Ph2PCH(Ph)CH(Me)NH2Me]Cl, (1R,2S)-Ph2<
Dahlenburg, Lutz,G?tz, Rainer
, p. 88 - 98 (2007/10/03)
The preparation of optically active β-aminophosphane ligands, (-)-(1R,2S)-Ph2PCH(Ph)CH(Me)NH2 (5), (+)-(1S,2S)-Ph2PCH(Ph)CH(Me)NH2 (6), (-)-(1R,2R)-Ph2PCH(Ph)CH(Me)NHMe (7), and (1R,2S)-Ph2
