582298-51-9 Usage
Uses
Used in Pharmaceutical Industry:
1-[(3aS,8aS)-tetrahydro-2,2-diMethyl-4,4,8,8-tetraphenyl-1,3-dioxolo[4,5-e][1,3,2]dioxaphosphepin-6-yl]-Pyrrolidine is used as a potential pharmaceutical compound for its unique molecular structure and the presence of phosphorus. Its complex nature may offer novel therapeutic applications, such as the development of new drugs or drug delivery systems.
Used in Materials Science:
In the field of materials science, 1-[(3aS,8aS)-tetrahydro-2,2-diMethyl-4,4,8,8-tetraphenyl-1,3-dioxolo[4,5-e][1,3,2]dioxaphosphepin-6-yl]-Pyrrolidine is used for its potential to contribute to the development of advanced materials with unique properties. Its complex structure and the presence of various functional groups may enable the creation of new materials with specific characteristics for various applications.
Used in Organic Synthesis:
1-[(3aS,8aS)-tetrahydro-2,2-diMethyl-4,4,8,8-tetraphenyl-1,3-dioxolo[4,5-e][1,3,2]dioxaphosphepin-6-yl]-Pyrrolidine is utilized as a key intermediate or building block in organic synthesis. Its complex structure and the presence of various functional groups make it a valuable component in the synthesis of other complex organic compounds, potentially leading to the discovery of new molecules with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 582298-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,2,2,9 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 582298-51:
(8*5)+(7*8)+(6*2)+(5*2)+(4*9)+(3*8)+(2*5)+(1*1)=189
189 % 10 = 9
So 582298-51-9 is a valid CAS Registry Number.
582298-51-9Relevant articles and documents
Ni-Catalyzed Asymmetric Cycloisomerization of Dienes by Using TADDOL Phosphoramidites
Schmitz, Christian,Leitner, Walter,Franciò, Giancarlo
supporting information, p. 10696 - 10702 (2015/07/20)
A library of α,α,α,α-tetraaryl-1,3-dioxolane-4,5-dimethanol (TADDOL)-based phosphoramidites has been synthesized and applied in the Ni-catalyzed cycloisomerization of different dienes. Through the systematic variation of the three structural motifs of the
Development, mechanism, and scope of the palladium-catalyzed enantioselective allene diboration
Burks, Heather E.,Liu, Shubin,Morken, James P.
, p. 8766 - 8773 (2008/02/12)
In the presence of a chiral phosphoramidite ligand, the palladium-catalyzed diboration of allenes can be executed with high enantioselectivity. This reaction provides high levels of selectivity with a range of aromatic and aliphatic allene substrates. Iso
Enantioselective rhodium-catalyzed [2+2+2] cycloaddition of alkenyl isocyanates and terminal alkynes: Application to the total synthesis of (+)-lasubine II
Yu, Robert T.,Rovis, Tomislav
, p. 12370 - 12371 (2007/10/03)
The use of TADDOL-based phosphoramidite ligands on rhodium allows for the incorporation of terminal alkynes in the [2+2+2] cycloaddition with alkenyl isocyanates. Terminal aliphatic alkynes provide bicyclic lactams, while the use of aryl alkynes provides complementary access to vinylogous amides. Product selectivity seems to be governed by a combination of electronics and sterics, with smaller and/or more electron-deficient substituents favoring lactam formation. The use of homologous alkenyl isocyanates leads to an expedient asymmetric total synthesis of the alkaloid lasubine II. Copyright
