444413

N-(tert-Butoxycarbonyl)-L-valinol

96%

• Lineare Formel: (CH₃)₂CHCH[NHCO₂C(CH₃)₃]CH₂OH
• CAS-Nummer: 79069-14-0
• Molekulargewicht: 203.28
• MDL-Nummer: MFCD00082635
• UNSPSC-Code: 12352209
• PubChem Substanz-ID: 24868123
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 100
• Assay: 96%
• Form: liquid
• Optische Aktivität: [α]23/D −23°, c = 1 in chloroform
• Eignung der Reaktion: reaction type: solution phase peptide synthesis
• Brechungsindex: n20/D 1.449 (lit.)
• bp: 208 °C (lit.)
• Dichte: 0.995 g/mL at 25 °C (lit.)
• Anwendung(en): 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
• InChIKey: OOQRRYDVICNJGC-MRVPVSSYSA-N

Beschreibung

Anwendung

Starting material for the synthesis of enantiopure homo-β-amino acids.[1][2] Used in the efficient synthesis of enantiopure tetrahydroisoquinolines.[3] Intermediate in the one-pot conversion of amino acid carbamates to N-derivatized 2-oxazolidinones.[4]

Sicherheitshinweise

• Lagerklassenschlüssel: 10 - Combustible liquids
• WGK: WGK 3
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type ABEK (EN14387) respirator filter