104057-64-9 Usage
Description
(2S,4S)-3-BENZOYL-2-T-BUTYL-4-METHYL-1,3-OXAZOLIDIN-5-ONE is a chiral chemical compound belonging to the oxazolidinone class, characterized by its molecular formula C16H21NO3. (2S,4S)-3-BENZOYL-2-T-BUTYL-4-METHYL-1,3-OXAZOLIDIN-5-ONE features a benzoyl group, a t-butyl group, and a methyl group, and is known for its two non-superimposable mirror image forms, referred to as enantiomers. Its unique molecular structure and reactivity contribute to its value as a versatile intermediate in the synthesis of complex organic compounds, particularly in the production of pharmaceuticals, agrochemicals, and other fine chemicals.
Uses
Used in Pharmaceutical Industry:
(2S,4S)-3-BENZOYL-2-T-BUTYL-4-METHYL-1,3-OXAZOLIDIN-5-ONE is used as a key building block in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the development of new drugs with specific therapeutic properties, contributing to advancements in medicine.
Used in Agrochemical Industry:
In the agrochemical sector, (2S,4S)-3-BENZOYL-2-T-BUTYL-4-METHYL-1,3-OXAZOLIDIN-5-ONE serves as an essential intermediate for the production of agrochemicals. Its incorporation into these compounds can lead to the creation of more effective and targeted pest control solutions.
Used in Organic Synthesis:
(2S,4S)-3-BENZOYL-2-T-BUTYL-4-METHYL-1,3-OXAZOLIDIN-5-ONE is utilized as a valuable intermediate in organic synthesis, enabling the construction of complex organic compounds with diverse applications across various industries. Its chiral nature and functional groups make it a preferred choice for creating enantioselective products and complex molecular architectures.
Check Digit Verification of cas no
The CAS Registry Mumber 104057-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,5 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104057-64:
(8*1)+(7*0)+(6*4)+(5*0)+(4*5)+(3*7)+(2*6)+(1*4)=89
89 % 10 = 9
So 104057-64-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H19NO3/c1-10-13(18)19-14(15(2,3)4)16(10)12(17)11-8-6-5-7-9-11/h5-10,14H,1-4H3/t10-,14-/m0/s1
104057-64-9Relevant articles and documents
Synthesis of Modified Partial Structures of the Bacterial Cell Wall. 2. Retarded Metabolism of Lipopeptides by Insertion of α-Substituted α-Amino Acids
Frauer, Alexandra,Mehlfuehrer, Michaela,Thirring, Klaus,Berner, Heinz
, p. 4215 - 4222 (2007/10/02)
The synthesis of the lipopeptide 1, which exhibits both immunological activity (induction of the colony stimulating factor (CSF) and stability against metabolic degradation, has been described.A detailed investigation of the course of the ene reaction bet
Synthese enantioselective d'α-aryl amino acides: subtitution nucleophile aromatique sur le fluorobenzene chrome tricarbonyle d'enolates chiraux
Chaari, M.,Jenhi, A.,Lavergne, J.-P.,Viallefont, Ph.
, p. C10 - C13 (2007/10/02)
We report here a convenient synthesis of optically pure α-aryl amino acids by enantioselective substitution of fluorobenzene tricarbonylchromium using the Schiff bases of L-alanine methyl ester with (1R,2R,5R)-2-hydroxy-3-pinanone in presence of LDA or deprotonated 2-(tert-butyl)-4-methyl-1,3-oxazolidin-5 one.