CAS 2899-29-8|L-Tryptophanol
| Common Name | L-Tryptophanol | ||
|---|---|---|---|
| CAS Number | 2899-29-8 | Molecular Weight | 190.24200 |
| Density | 1.245g/cm3 | Boiling Point | 444.2ºC at 760mmHg |
| Molecular Formula | C11H14N2O | Melting Point | 73-77 °C(lit.) |
| MSDS | ChineseUSA | Flash Point | 222.5ºC |
| Symbol | GHS07 | Signal Word | Warning |
Names
| Name | (2S)-2-amino-3-(1H-indol-3-yl)propan-1-ol |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Density | 1.245g/cm3 |
|---|---|
| Boiling Point | 444.2ºC at 760mmHg |
| Melting Point | 73-77 °C(lit.) |
| Molecular Formula | C11H14N2O |
| Molecular Weight | 190.24200 |
| Flash Point | 222.5ºC |
| Exact Mass | 190.11100 |
| PSA | 62.04000 |
| LogP | 1.73030 |
| Vapour Pressure | 1.13E-08mmHg at 25°C |
| Index of Refraction | -21 ° (C=1, MeOH) |
| InChIKey | UDQCRUSSQAXPJY-VIFPVBQESA-N |
| SMILES | NC(CO)Cc1c[nH]c2ccccc12 |
Safety Information
| Symbol | GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302 |
| Hazard Codes | Xi |
| Risk Phrases | R36/37/38 |
| Safety Phrases | S26-S36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
Articles8
More Articles| Enantioselective formal synthesis of (+)-dihydrocorynantheine and (-)-dihydrocorynantheol. J. Org. Chem. 74(3) , 1205-11, (2009) The enantioselective construction of the 3-ethylindolo[2,3-a]quinolizidine moiety present in numerous indole alkaloids is reported, the key steps being a stereoselective cyclocondensation of (S)-trypt... | |
| Straightforward methodology for the enantioselective synthesis of benzo[a]- and indolo[2,3-a]quinolizidines. J. Org. Chem. 72(14) , 5193-201, (2007) An enantioselective two-step route to substituted benzo[a]- and indolo[2,3-a]quinolizidines has been developed. It consists of (i) a stereoselective cyclocondensation of a racemic or prochiral delta-o... | |
| Enantioselective formal synthesis of ent-rhynchophylline and ent-isorhynchophylline. Chem. Commun. (Camb.) 49(19) , 1954-6, (2013) Starting from (S)-tryptophanol, a formal synthesis of ent-rhynchophylline and ent-isorhynchophylline, involving stereoselective cyclocondensation, spirocyclization, and alkylation reactions, and the f... |
Synonyms
| (2S)-2-Amino-3-(1H-indol-3-yl)-1-propanol |
| L-(-)-Tryptophanol |
| (S)-(-)-2-Amino-3-(3-indolyl)propanol |
| H-Tryptophanol |
| 2-amino-3-(1H-indol-3-yl)propan-1-ol |
| 1H-Indole-3-propanol, β-amino-, (βS)- |
| L-Tryptophanol |
| (2S)-2-amino-3-(1H-indol-3-yl)propan-1-ol |
| Tryptophanol |
| MFCD00037970 |
| L-Trp-ol |
