62965-56-4

Basic information

• Product Name: (S)-(-)-4-tert-Butyloxazolidine-2,5-dione
• Synonyms: L-TERT-LEUCINE NCA;(S)-4-TERT-BUTYLOXAZOLIDINE-2,5-DIONE;L-tert-Leucine N-carboxyanhydride
• CAS NO: 62965-56-4
• Molecular Formula: C₇H₁₁NO₃
• Molecular Weight: 157.17
• EINECS: -0
• Product Categories: Leucine [Leu, L]
• Mol File: 62965-56-4.mol
• Article Data: 2

Chemical Properties

• Melting Point: 132°C
• Appearance: /
• Density: 1.164g/cm³
• Refractive Index: 1.464
• Water Solubility: Slightly soluble in water.
• Sensitive: Moisture Sensitive
• BRN: 4664497
• CAS DataBase Reference: (S)-(-)-4-tert-Butyloxazolidine-2,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(-)-4-tert-Butyloxazolidine-2,5-dione(62965-56-4)
• EPA Substance Registry System: (S)-(-)-4-tert-Butyloxazolidine-2,5-dione(62965-56-4)

Safety Data

• Safety Statements: S22:Do not inhale dust.; S24/25:Avoid contact with skin and eyes.
• Hazardous Substances Data: 62965-56-4(Hazardous Substances Data)

Usage

Uses

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

InChI:InChI=1/C7H11NO3/c1-7(2,3)4-5(9)11-6(10)8-4/h4H,1-3H3,(H,8,10)

Upstream product

• 75-44-5 phosgene 
• 20859-02-3 L-tert-Leucine 
• 70874-05-4 Z-D-Tle 

Downstream Products

• 13007-90-4 bis(triphenylphosphine)nickel⁽⁰⁾ dicarbonyl 
• 67151-54-6 N-acetyl-L-tert-leucine N'-methylamide 
• 63009-42-7 (R)-2-((S)-2-Amino-3,3-dimethyl-butyrylamino)-3-phenyl-propionic acid methyl ester 
• 84907-94-8 (2R,5S)-2-Benzyl-5-tert-butyl-3,6-dimethoxy-2,5-dihydro-pyrazine 
• 65050-07-9 Cyclo(L-tert-Leu-Gly) 
• 63038-26-6 (S)-2-amino-3,3-dimethyl-butyric acid methyl ester 
• 89226-12-0 L-tert-leucine methylamide 
• 62965-57-5 (S)-(+)-2-amino-3,3-dimethylbutanamide 

Relevant articles and documents

ENANTIOSELECTIVE SYNTHESIS OF NON-PROTEINOGENIC AMINO ACIDS VIA METALLATED BIS-LACTIM ETHERS OF 2,5-DIKETOPIPERAZINES

Bis-lactim ethers 1 of 2,5-diketopiperazines contain a chiral inducing center, an acidic CH-bond and two sites susceptible to hydrolysis.They react with BuLi to give Li compounds of type 4, 15, 29 or 32, which possess a prochiral C atom.They readily add electrophiles (such as alkylating agents or carbonyl compounds) with unusually high diastereoface differentiation.In many cases the d.e-value (d.e. = diastereomeric excess = asymmetric induction) of the adduct exceeds 95percent.On hydrolysis the adducts are cleaved liberating the chiral auxiliary (used to build up the bis-lactim ether 1) and the target molecules, the optically active amino acid methyl esters of type 8, 19, 25 or 36.The two amino acid esters are separable either by fractional distillation or (eventually after further hydrolysis to amino acids) by chromatography.Transition state models are discussed that could explain the exceptionally high asymmetric induction and the predictability of the induced configuration.