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L-tert-Leucine

ALDRICH/269107 - 99%

Synonym: (S)-2-Amino-3,3-dimethylbutyric acid; L-α-tert-Butylglycine

CAS Number: 20859-02-3
Empirical Formula (Hill Notation): C6H13NO2
Molecular Weight: 131.17
MDL Number: MFCD00064218
Linear Formula: (CH3)3CCH(NH2)CO2H
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-269107-5G 5 g
$114.00
1/EA
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45-269107-25G 25 g
$183.00
1/EA
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application(s) peptide synthesis
assay 99%
form powder
InChI 1S/C6H13NO2/c1-6(2,3)4(7)5(8)9/h4H,7H2,1-3H3,(H,8,9)/t4-/m1/s1
InChI key NPDBDJFLKKQMCM-SCSAIBSYSA-N
mp ≥300 °C (lit.)
optical activity [α]20/D −9.5°, c = 3 in H2O
optical purity ee: 99% (GLC)
Quality Level 200 
reaction suitability reaction type: solution phase peptide synthesis
SMILES string CC(C)(C)[C@H](N)C(O)=O
Application: L-tert-Leucine can be used:
• As a key precursor in the synthesis of a chiral phosphinooxazoline ligand, (S)-tert-butylPHOX.
• In the synthesis of chiral copper(II) polymers that can catalyze the kinetic resolution of secondary alcohols by acylation.
• In metal-free tandem radical cyclization reactions to synthesize 6-alkyl/acyl phenanthridines.
• In the preparation of tert-leucine-derived N-acetylthiazolidinethione auxiliary that provides high levels of diastereoselection in acetate aldol reactions with a variety of aldehydes.

General description: L-tert-Leucine is an amino acid used as a precursor for synthesizing chiral tridentate Schiff base ligands.
Packaging: 5, 25 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 1
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity 99%
mp ≥300 °C (lit.)
UNSPSC 12352209

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