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Quality Level
Assay
96%
form
liquid
optical activity
[α]23/D −23°, c = 1 in chloroform
reaction suitability
reaction type: solution phase peptide synthesis
refractive index
n20/D 1.449 (lit.)
bp
208 °C (lit.)
density
0.995 g/mL at 25 °C (lit.)
application(s)
peptide synthesis
SMILES string
CC(C)[C@@H](CO)NC(=O)OC(C)(C)C
InChI
1S/C10H21NO3/c1-7(2)8(6-12)11-9(13)14-10(3,4)5/h7-8,12H,6H2,1-5H3,(H,11,13)/t8-/m1/s1
InChI key
OOQRRYDVICNJGC-MRVPVSSYSA-N
Application
Starting material for the synthesis of enantiopure homo-β-amino acids. Used in the efficient synthesis of enantiopure tetrahydroisoquinolines. Intermediate in the one-pot conversion of amino acid carbamates to N-derivatized 2-oxazolidinones.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Tetrahedron Letters, 35, 9533-9533 (1994)
Synthesis, 1331-1331 (1994)
Tetrahedron, 51, 12337-12337 (1995)
Tetrahedron Letters, 36, 167-167 (1995)
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