tert-butyl [(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate
N-(tert-butoxycarbonyl)-L-valinol
CAS: 79069-14-0
Molecular Formula: C10H21NO3
tert-butyl [(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate - Names and Identifiers
| Name | N-(tert-butoxycarbonyl)-L-valinol |
| Synonyms | BOC-VAL-OL Boc-Val-ol BOC-VALINOL BOC-L-VAL-OL BOC-L-VALINOL N-Boc-L-Valinol N-Boc-L-valinol N-(tert-butoxycarbonyl)-L-valinol BOC-(S)-2-AMINO-3-METHYL-1-BUTANOL NALPHA-tert-Butoxycarbonyl-L-valinol N-tert-Butoxycarbonyl-(S)-2-amino-3-methyl-1-butanol tert-butyl [(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate Carbamic acid, (1S)-1-(hydroxymethyl)-2-methylpropyl-, 1,1-dimethylethyl ester Boc-Val-ol~N-tert-Butoxycarbonyl-(S)-2-amino-3-methyl-1-butanol~N-(tert-Butoxycarbonyl)-L-valinol |
| CAS | 79069-14-0 |
| InChI | InChI=1/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 |
tert-butyl [(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate - Physico-chemical Properties
| Molecular Formula | C10H21NO3 |
| Molar Mass | 203.28 |
| Density | 0.995g/mLat 25°C(lit.) |
| Boling Point | 208°C(lit.) |
| Specific Rotation(α) | -23 º (c=1 in chloroform) |
| Flash Point | 185°F |
| Vapor Presure | 9.15E-05mmHg at 25°C |
| BRN | 4663728 |
| pKa | 12.02±0.46(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | n20/D 1.449(lit.) |
tert-butyl [(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| UN IDs | NA 1993 / PGIII |
| WGK Germany | 3 |
| HS Code | 29224999 |
tert-butyl [(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate - Reference Information
| use | raw materials for synthesizing enantiomeric β-high amino acids. It is used for the efficient synthesis of enantiomeric pure tetrahydroisoquinoline. One-pot conversion of amino acid carbamates to intermediates of N-derived 2-azolidinone. |
Last Update：2024-04-10 22:41:56
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