1092491-37-6 Usage
Uses
Used in Organic Synthesis:
(S)-4-tert-butyl-2-(2-(bis(3,5-bis(trifluoromethyl)phenyl)phosphino)phenyl)-4,5-dihydrooxazole is used as a building block in organic synthesis for the creation of more complex molecules due to its versatile functional groups and unique structure.
Used in Catalysis:
In the field of catalysis, (S)-4-tert-butyl-2-(2-(bis(3,5-bis(trifluoromethyl)phenyl)phosphino)phenyl)-4,5-dihydrooxazole is used as a catalyst or a catalyst precursor to facilitate various chemical reactions, potentially improving reaction rates and selectivity.
Used in Pharmaceutical Industry:
(S)-4-tert-butyl-2-(2-(bis(3,5-bis(trifluoromethyl)phenyl)phosphino)phenyl)-4,5-dihydrooxazole is used as an active pharmaceutical ingredient or a key intermediate in the development of new drugs, leveraging its complex structure to target specific biological receptors or enzymes.
Used in Molecular Recognition:
In the field of molecular recognition, (S)-4-tert-butyl-2-(2-(bis(3,5-bis(trifluoromethyl)phenyl)phosphino)phenyl)-4,5-dihydrooxazole is used as a molecular probe or a component in the design of new receptors, taking advantage of its unique structural features to recognize and bind target molecules with high specificity.
Used in Materials Science:
(S)-4-tert-butyl-2-(2-(bis(3,5-bis(trifluoromethyl)phenyl)phosphino)phenyl)-4,5-dihydrooxazole is used in materials science as a component in the development of new materials with specialized properties, such as improved conductivity, strength, or stability, due to its distinctive molecular architecture.
Check Digit Verification of cas no
The CAS Registry Mumber 1092491-37-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,4,9 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1092491-37:
(9*1)+(8*0)+(7*9)+(6*2)+(5*4)+(4*9)+(3*1)+(2*3)+(1*7)=156
156 % 10 = 6
So 1092491-37-6 is a valid CAS Registry Number.
1092491-37-6Relevant articles and documents
Enantioselective Intermolecular Addition of Aliphatic Amines to Acyclic Dienes with a Pd-PHOX Catalyst
Adamson, Nathan J.,Hull, Ethan,Malcolmson, Steven J.
supporting information, p. 7180 - 7183 (2017/06/05)
We report a method for the catalytic, enantioselective intermolecular addition of aliphatic amines to acyclic 1,3-dienes. In most cases, reactions proceed efficiently at or below room temperature in the presence of 5 mol % of a Pd catalyst bearing a PHOX ligand, generating allylic amines in up to 97:3 er. The presence of an electron-deficient phosphine within the ligand not only leads to a more active catalyst but also is critical for achieving high site selectivity in the transformation.
Asymmetric palladium-catalyzed intramolecular α-arylation of aldehydes
Garcia-Fortanet, Jorge,Buchwald, Stephen L.
supporting information; experimental part, p. 8108 - 8111 (2009/04/13)
(Chemical Equation Presented) Phoxy ligand: The first catalytic method for the asymmetric palladium-catalyzed intramolecular α-arylation of α-branched aldehydes was developed (see scheme). This process is distinguished by the high yields and enantioselectivities that can be obtained, making this protocol a useful synthetic tool for further applications.
