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104057-64-9

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104057-64-9 Usage

General Description

"(2S,4S)-3-BENZOYL-2-T-BUTYL-4-METHYL-1,3-OXAZOLIDIN-5-ONE" is a chemical compound with the molecular formula C16H21NO3. It is a member of the oxazolidinone class of compounds and contains a benzoyl group, a t-butyl group, and a methyl group. (2S,4S)-3-BENZOYL-2-T-BUTYL-4-METHYL-1,3-OXAZOLIDIN-5-ONE is a chiral molecule, meaning it has two non-superimposable mirror image forms, known as enantiomers. It is commonly used in organic synthesis as a building block for the production of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique molecular structure and reactivity make it a valuable intermediate in the synthesis of complex organic compounds.

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

104057-64-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4S)-3-benzoyl-2-tert-butyl-4-methyl-1,3-oxazolidin-5-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:104057-64-9 SDS

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.

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