Boc-L-valinol

CAS: 79069-14-0

Ref. 3D-FB47647

Product Information

• Name: Boc-L-valinol
• Synonyms: Boc-L-Val-ol, (1S)-N-(tert-Butoxycarbonyl)-1-isopropyl-2-hydroxyethylamine, (2S)-2-[(tert-Butyloxycarbonyl)amino]-3-methylbutan-1-ol, (S)-(-)-2-(tert-Butoxycarbonylamino)-3-methyl-1-butanol, (S)-tert-Butyl 1-hydroxy-3-methylbutan-2-ylcarbamate, 1,1-Dimethylethyl N-[(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate, Boc-Val-ol, Carbamic acid, N-[(1S)-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-dimethylethyl ester, Carbamic acid, [(1S)-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-dimethylethyl ester, Carbamic acid, [1-(hydroxymethyl)-2-methylpropyl]-, 1,1-dimethylethyl ester, (S)-, N-Boc-(S)-valinol, N-Boc-L-valinol, N-tert-Butoxycarbonyl-(S)-2-amino-3-methyl-1-butanol, N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-valinol, N-tert-Butoxycarbonylo-(S)-valinol, NALPHA-tert-Butoxycarbonyl-L-valinol, tert-Butyl N-[(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate, tert-Butyloxycarbonyl-(S)-valinol, tert-butyl [(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate

Description

Boc-L-valinol is a chiral amino acid that is a hybridization agent. It can be used in the synthesis of sulfonic acids, malonates, and cinchona alkaloids. This compound has been shown to catalyze epoxidation reactions as well as alkylation reactions with alcohols and thiols. Boc-L-valinol can also be used in the synthesis of nucleophilic monomers that have modifications in their functional groups. The molecular modeling of this compound has shown that it is able to act as a nucleophile in its monomer form.

• Brand: Biosynth

Chemical properties

• Molecular weight: 203.28 g/mol
• Formula: C₁₀H₂₁NO₃
• Purity: Min. 95%
• InChI: 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: InChIKey=OOQRRYDVICNJGC-MRVPVSSYSA-N
• SMILES: CC(C)[C@@H](CO)NC(=O)OC(C)(C)C