1642865-72-2 Usage
Uses
Used in Chemical Synthesis:
(11bS)-2,6-diphenyl-N,N-bis((R)-1-phenylethyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine is used as a key intermediate in the synthesis of complex organic molecules, particularly in the pharmaceutical and chemical industries. Its unique structure and composition make it a valuable building block for the development of new compounds with potential applications in various fields.
Used in Catalysis:
Due to its intricate structure and potentially unique properties, (11bS)-2,6-diphenyl-N,N-bis((R)-1-phenylethyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine can be employed as a catalyst in various chemical reactions. Its ability to facilitate specific transformations can be beneficial in enhancing the efficiency and selectivity of these processes.
Used in Pharmaceutical Research:
(11bS)-2,6-diphenyl-N,N-bis((R)-1-phenylethyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine is used as a starting material or a component in the development of new pharmaceutical compounds. Its unique structure may provide novel opportunities for drug discovery and the design of innovative therapeutic agents.
Used in Organic Chemistry:
In the field of organic chemistry, (11bS)-2,6-diphenyl-N,N-bis((R)-1-phenylethyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine is used for the synthesis of complex organic molecules. Its presence in reactions can lead to the formation of new compounds with potential applications in various industries, such as materials science, agrochemicals, and fragrances.
Check Digit Verification of cas no
The CAS Registry Mumber 1642865-72-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,2,8,6 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1642865-72:
(9*1)+(8*6)+(7*4)+(6*2)+(5*8)+(4*6)+(3*5)+(2*7)+(1*2)=192
192 % 10 = 2
So 1642865-72-2 is a valid CAS Registry Number.
1642865-72-2Relevant academic research and scientific papers
Chang, Rui,Cai, Shoule,Yang, Guoqing,Yan, Xuyang,Huang, Hanmin
, p. 12467 - 12472 (2021)
The asymmetric construction of allylic C-O bonds with primary or secondary aliphatic alcohols remains a substantial challenge in Pd-catalyzed allylation chemistry. Here, we report the development of an additive-free, palladium-catalyzed asymmetric aminomethylative etherification of conjugated dienes that enables the efficient, asymmetric O-allylation of primary and secondary aliphatic alcohols as well as water. Mechanism studies revealed that the hydrogen-bonding interaction between the alcohol and the in situ introduced aminomethyl moiety is critical to facilitate the nucleophilic addition of the alcohol to the π-allylpalladium species, which opened up the possibility of using aliphatic alcohols and water as nucleophilic substrates. This reaction tolerates a broad range of functional groups and shows remarkable regioselectivities and uniformly high enantioselectivities, which provides a direct and rapid approach to optically pure allylic 1,3-amino ethers and 1,3-amino alcohols from simple starting materials.
