| Identification | More | [Name]
(S)-(-)-1-Boc-2-pyrrolidinemethanol | [CAS]
69610-40-8 | [Synonyms]
BOC-L-PROLINOL
BOC-L-PRO-OL
BOC-PROLINOL
BOC-PRO-OL
BOC-(S)-2-(HYDROXYMETHYL) PYRROLIDINE
BOS-(S)-2-(HYDROXYMETHYL)PYRROLIDINE
N-ALPHA-T-BOC-L-PROLINOL
N-ALPHA-T-BUTYLOXYCARBONYL-L-PROLINOL
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-PROLINOL
N-BOC-L-PROLINOL
N-T-BOC-L-PROLINOL
N-T-BUTOXYCARBONYL-L-PROLINOL
N-TERT-BUTOXYCARBONYL-L-PROLINOL
(S)-(-)-1-BOC-2-PYRROLIDINEMETHANOL
(S)-1-BOC-2-PYRROLIDINEMETHANOL
(S)-(-)-1-(TERT-BUTOXYCARBONYL)-2-PYRROLIDINEMETHANOL
(S)-2-HYDROXYMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
(S)-(-)-N-BOC-PROLINOL
(S)-(+)-N-BOC-PROLINOL
(S)-N-TERT-BUTOXYCARBONYL PROLINOL | [EINECS(EC#)]
627-775-3 | [Molecular Formula]
C10H19NO3 | [MDL Number]
MFCD00066232 | [Molecular Weight]
201.26 | [MOL File]
69610-40-8.mol |
| Chemical Properties | Back Directory | [Appearance]
White powder | [Melting point ]
62-64 °C (lit.) | [alpha ]
-52 º (c=1, CHCl3) | [Boiling point ]
150 °C / 4mmHg | [density ]
1.0948 (rough estimate) | [refractive index ]
-55 ° (C=5, MeOH) | [storage temp. ]
Store at 0°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly), Water (Slightly) | [form ]
Crystalline Powder | [pka]
14.77±0.10(Predicted) | [color ]
White | [optical activity]
[α]21/D 48°, c = 1.3 in chloroform | [Water Solubility ]
insoluble | [Detection Methods]
T,NMR,HPLC,Rotation | [BRN ]
3542667 | [InChIKey]
BFFLLBPMZCIGRM-QMMMGPOBSA-N | [CAS DataBase Reference]
69610-40-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
Building block for novel nicotinic acetylcholine receptor ligands with cognition-enhancing properties. Used in the synthesis of chiral β-amino sulfides and β-amino thiols. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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