Name | Fmoc-S-trityl-L-Cysteine |
Synonyms | FMOC-CYS(TRT) FMOC-L-CYS(TRT) Fmoc-Cys(Trt)-OH FMOC-CYS(TRT)-OH FMOC-L-CYS(TRT)-OH FMOC-L-CYS(TRITYL) FMOC-CYSTEINE(TRT)-OH FMOC-L-CYSTEINE (TRT) FMOC-L-CYSTEINE(TRITYL) Fmoc-L-Cysteine(Trityl) Fmoc-S-trityl-L-Cysteine N-(9-Fluorenyl Methoxy Carbonyl)-S-Trityl-L-Cysteine N-[(9H-fluoren-9-ylmethoxy)carbonyl]-S-trityl-L-cysteine N-[(9H-fluoren-9-ylmethoxy)carbonyl]-S-trityl-D-cysteine 2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-(tritylthio)propanoic acid (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-(tritylsulfanyl)propanoate (2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-(tritylsulfanyl)propanoate |
CAS | 103213-32-7 |
EINECS | 600-408-4 |
InChI | InChI=1/C37H31NO4S/c39-35(40)34(38-36(41)42-24-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33)25-43-37(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28/h1-23,33-34H,24-25H2,(H,38,41)(H,39,40)/t34-/m1/s1 |
InChIKey | KLBPUVPNPAJWHZ-UMSFTDKQSA-N |
Molecular Formula | C37H31NO4S |
Molar Mass | 585.71 |
Density | 1.270±0.06 g/cm3(Predicted) |
Melting Point | 170-173°C(lit.) |
Boling Point | 763.4±60.0 °C(Predicted) |
Specific Rotation(α) | 16 º (c=1, THF) |
Flash Point | 415.5°C |
Water Solubility | Insoluble in water. Soluble in most organic solvents. |
Vapor Presure | 1.68E-24mmHg at 25°C |
Appearance | White solid |
Color | White to almost white |
BRN | 4221286 |
pKa | 3.70±0.10(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 18 ° (C=1, THF) |
MDL | MFCD00038538 |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
FLUKA BRAND F CODES | 9-21 |
HS Code | 29309090 |
Hazard Note | Irritant |
application | Fmoc-S-trityl-L-cysteine is an organic synthesis intermediate, which can be used for synthesis of amino acid derivatives, mainly used in laboratory research and development process and biochemical production process. |