Name | N-alpha-t-BOC-o-benzyl-L-serine |
Synonyms | Boc-Ser(Bzl)-OH Boc-Ser(Bz1)-OH N-BOC-O-Benzyl-L-ser N-BOC-O-BENZYL-SERINE N-Boc-O-benzyl-L-serine N-alpha-t-BOC-o-benzyl-L-serine L-SERINE-N-T-BOC, O-BZ ETHER (15N) L-SERINE-N-T-BOC, O-BZ ETHER (2-13C) N-Boc-O-benzyl-L-serineBoc-Ser(Bzl)-OH O-benzyl-N-(tert-butoxycarbonyl)serine Nα-tert-Butoxycarbonyl-O-benzyl-L-serine (2S)-3-Benzyloxy-2-(tert-butoxycarbonylamino)propanoic acid (2S)-3-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]propanoate (S)-3-(benzyloxy)-2-((tert-butoxycarbonyl)aMino)propanoic acid |
CAS | 23680-31-1 |
EINECS | 245-820-1 |
InChI | InChI=1/C15H21NO5/c1-15(2,3)21-14(19)16-12(13(17)18)10-20-9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/p-1/t12-/m0/s1 |
InChIKey | DMBKPDOAQVGTST-LBPRGKRZSA-N |
Molecular Formula | C15H21NO5 |
Molar Mass | 295.33 |
Density | 1.1454 (rough estimate) |
Melting Point | 58-60°C(lit.) |
Boling Point | 437.02°C (rough estimate) |
Specific Rotation(α) | 21.5 º (c=2, ethanol) |
Flash Point | 229.7°C |
Vapor Presure | 4.07E-09mmHg at 25°C |
Appearance | White crystal or powder |
Color | White to Almost white |
BRN | 3064461 |
pKa | 3.53±0.10(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Refractive Index | 22 ° (C=2, EtOH) |
MDL | MFCD00066063 |
Physical and Chemical Properties | White crystalline powder; Insoluble in water and petroleum ether, soluble in ethyl acetate, acetic acid and ethanol; mp is 56-58 ℃; Specific optical rotation [α]20D 20 °(0.5-2.0 mg/ml, acetic acid). |
Hazard Symbols | Xn - Harmful |
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S24/25 - Avoid contact with skin and eyes. S36 - Wear suitable protective clothing. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 2924 29 70 |
Hazard Class | IRRITANT |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Use | Used for polypeptide synthesis and as an amino acid protective monomer. |
Production method | Suspended O-benzyl-L-serine in dioxane solution, acylation with tert-butoxycarbonyl azide to obtain a crude product, extracted with ethyl acetate at pH 9-10, and then refined by recrystallization. |