1435467-28-9 Usage
Description
(3aS,3a'S,8aR,8a'R)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole) is a complex organic molecule that belongs to the oxazole family. It features a unique fused indeno-oxazole ring system and contains elements such as carbon, hydrogen, and oxygen. The presence of tert-butyl and phenyl groups in its structure contributes to its steric and electronic properties, which may have potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(3aS,3a'S,8aR,8a'R)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole) is used as a potential pharmaceutical compound for its unique structure and properties. Its steric and electronic characteristics due to the presence of tert-butyl and phenyl groups may contribute to its interaction with biological targets, making it a candidate for drug development.
Used in Materials Science:
In the field of materials science, (3aS,3a'S,8aR,8a'R)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole) may be utilized for the development of new materials with specific properties. Its unique structure and the presence of various functional groups could be exploited to create materials with tailored characteristics for various applications.
Used in Organic Synthesis:
(3aS,3a'S,8aR,8a'R)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole) can be employed as a synthetic building block or intermediate in organic synthesis. Its complex structure and the presence of multiple functional groups make it a potentially useful component in the synthesis of other organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.
Note: The specific applications and uses mentioned above are hypothetical and would require further research and investigation to confirm their validity and practicality.
Check Digit Verification of cas no
The CAS Registry Mumber 1435467-28-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,5,4,6 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1435467-28:
(9*1)+(8*4)+(7*3)+(6*5)+(5*4)+(4*6)+(3*7)+(2*2)+(1*8)=169
169 % 10 = 9
So 1435467-28-9 is a valid CAS Registry Number.
1435467-28-9Relevant articles and documents
Catalytic Asymmetric Fluorination of Copper Carbene Complexes: Preparative Advances and a Mechanistic Rationale
Buchsteiner, Michael,Fürstner, Alois,Jerabek, Paul,Lehmann, Christian W.,Martinez-Rodriguez, Luis,N?thling, Nils,Patzer, Michael,Pozo, Iago
supporting information, p. 2509 - 2515 (2020/02/26)
The Cu-catalyzed reaction of substituted α-diazoesters with fluoride gives α-fluoroesters with ee values of up to 95 %, provided that chiral indane-derived bis(oxazoline) ligands are used that carry bulky benzyl substituents at the bridge and moderately bulky isopropyl groups on their core. The apparently homogeneous solution of CsF in C6F6/hexafluoroisopropanol (HFIP) is the best reaction medium, but CsF in the biphasic mixture CH2Cl2/HFIP also provides good results. DFT studies suggest that fluoride initially attacks the Cu- rather than the C-atom of the transient donor/acceptor carbene intermediate. This unusual step is followed by 1,2-fluoride shift; for this migratory insertion to occur, the carbene must rotate about the Cu?C bond to ensure orbital overlap. The directionality of this rotatory movement within the C2-symmetric binding site determines the sense of induction. This model is in excellent accord with the absolute configuration of the resulting product as determined by X-ray diffraction using single crystals of this a priori wax-like material grown by capillary crystallization.
