| Name | (2S)-4-cyclohexyloxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxobutanoic acid |
|---|---|
| Synonyms |
(9H-Fluoren-9-yl)MethOxy]carbonyl Asp(OcHex)-OH
FMOC-L-ASPATIC ACID-B-CYCLOHEXYLESTER FMOC-ASP(OCHEX)-OH N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-ASPTIC ACID BETA-CYCLOHEXYL ESTER Fmoc-Asp(OcHex)-OH FMOC-AAP(OCHEX)-OH FMOC-ASP(OCHEX)-OH //BP Fmoc-L-asptic acid-β-cyclohexyl ester FMOC-L-ASP(OCHX)-OH N-Fmoc-L-aspticacid4-cyclohexylester FMOC-ASP(OCHX)-OH N-Fmoc-L-asptic acid 4-cyclohexyl ester FMOC-L-ASPTIC ACID -4 CYCLOHEXYL ESTER FMOC-L-ASP(CHX)-OH FMOC-ASP-(OCHX)-PH (3S)-4-(Cyclohexyloxy)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid FMOC-L-ASPTIC ACID BETA-CYCLOHEXYL ESTER L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1-cyclohexyl ester FMoc-Asp(OcHx)-OH FMoc-L-asptic acid β-cyclohexyl ester (2S)-4-cyclohexyloxy-2-(9H-fluoren-9-ylmethoxycbonylamino)-4-oxobutanoicaci 4-cyclohexyloxy-2-[[9H-fluoren-9-ylmethoxy(oxo)methyl]amino]-4-oxobutanoic acid (2S)-4-(Cyclohexyloxy)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid FMOC-L-ASPATIC ACID-BETA-CYCLOHEXYL ESTER L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-cyclohexyl ester Fmoc-L-asptic acid-β-cyclohexyl ester (HPLC) L-Asptic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-cyclohexyl ester Fmoc-L-aspartic acid 4-cyclohexyl ester (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(cyclohexyloxy)-4-oxobutanoic acid Fmoc-L-Asp(OcHex)-OH NALPHA-9-Fluorenylmethoxycbonyl-L-asptic acid B-cyclohexyl ester Fmoc-L-asptic acid β-cyclohexyl ester N-9-Fluorenylmethoxycbonyl-L-asptic acid cyclohexyl ester AmbotzFAA1705 N-9-FLUORENYLMETHYLOXYCBONYL-L-ASPTIC ACID 4-CYCLOHEXYL ESTER (2S)-4-(cyclohexyloxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid N-alpha-FMoc-L-asptic acid-beta-cyclohexyl ester FMOC-ASPTIC ACID(OCHEX) N-ALPHA-(9-FLUORENYLMETHYLOXYCBONYL)-L-ASPTIC ACID BETA-CYCLOHEXYL ESTER Fmoc-Asn(OcHex)-OH MFCD00135420 |
| Description | Fmoc-Asp(OcHex)-OH is an aspartic acid derivative[1]. |
|---|---|
| Related Catalog | |
| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
| References |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 664.4±55.0 °C at 760 mmHg |
| Molecular Formula | C25H27NO6 |
| Molecular Weight | 437.485 |
| Flash Point | 355.6±31.5 °C |
| Exact Mass | 437.183838 |
| PSA | 101.93000 |
| LogP | 5.99 |
| Vapour Pressure | 0.0±2.1 mmHg at 25°C |
| Index of Refraction | 1.617 |
| Storage condition | -15°C |
| Hazard Codes | Xi |
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