CAS 79069-50-4|Boc-L-alaninal
| Common Name | Boc-L-alaninal | ||
|---|---|---|---|
| CAS Number | 79069-50-4 | Molecular Weight | 173.210 |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 248.5±23.0 °C at 760 mmHg |
| Molecular Formula | C8H15NO3 | Melting Point | 89 °C |
| MSDS | USA | Flash Point | 104.1±22.6 °C |
Names
| Name | tert-butyl N-[(2S)-1-oxopropan-2-yl]carbamate |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Density | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 248.5±23.0 °C at 760 mmHg |
| Melting Point | 89 °C |
| Molecular Formula | C8H15NO3 |
| Molecular Weight | 173.210 |
| Flash Point | 104.1±22.6 °C |
| Exact Mass | 173.105194 |
| PSA | 55.40000 |
| LogP | 1.23 |
| Appearance of Characters | Powder | White to yellow |
| Vapour Pressure | 0.0±0.5 mmHg at 25°C |
| Index of Refraction | 1.436 |
| InChIKey | OEQRZPWMXXJEKU-LURJTMIESA-N |
| SMILES | CC(C=O)NC(=O)OC(C)(C)C |
| Storage condition | −20°C |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
Articles3
More Articles| Synthesis of the C(26)-C(32) Oxazole Fragment of Calyculin C: A Test Case for Oxazole Syntheses. J. Org. Chem. 63 , 92-98, (1998) The synthesis of the C(26)-C(32) oxazole fragment 4 and its C(32) epimer 20 of serine/threonine protein phosphatase PP1 and PP2A inhibitor calyculin C is presented. The syn methyl arrangement in 4 was... | |
| Synthesis of a C20-C26 segment of superstolide A by addition of a chiral allenylzinc reagent to (R)-N-boc alaninal. Org. Lett. 7 , 1593-1596, (2005) [reaction: see text] Additions of chiral allenylzinc and indium reagents to N-Boc alaninal were examined as a possible route to a C20-C26 segment of superstolide A. Allenylzinc reagents, prepared in s... | |
| Practical syntheses of a CXCR3 antagonist. J. Org. Chem. 76 , 1767-1774, (2011) Two new, reliable syntheses of a pyrido[2,3-d]-pyrimidine inhibitor of the CXCR3 receptor are described. A nine-step synthesis of the CXCR3 inhibitor (1) from 2-aminonicotinic acid was demonstrated on... |
Synonyms
| tert-Butyl [(2S)-1-oxopropan-2-yl]carbamate |
| Boc-L-alanine aldehyde |
| (S)-tert-Butyl (1-oxopropan-2-yl)carbamate |
| Carbamic acid, N-[(1S)-1-methyl-2-oxoethyl]-, 1,1-dimethylethyl ester |
| Boc-alaninal |
| Boc-Ala-Aldehyde |
| 2-Methyl-2-propanyl (1-oxo-2-propanyl)carbamate |
| N-T-BOC-L-ALANINAL |
| 2-Methyl-2-propanyl [(2S)-1-oxo-2-propanyl]carbamate |
| N-Boc-L-alaninal |
| Boc-L-alaninal |
| boc-L-alanine |
| Carbamic acid, N-(1-methyl-2-oxoethyl)-, 1,1-dimethylethyl ester |
| Boc-Ala-H |
