| Name | (4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-prop-2-enoxypentanoic acid |
|---|---|
| Synonyms |
(4S)-4-(9H-fluoren-9-ylmethoxycbonylamino)-5-oxo-5-prop-2-enoxypentanoicaci
(S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(allyloxy)-5-oxopentanoic acid Fmoc-L-glutamic acid α-allyl ester (4S)-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-5-oxo-5-(prop-2-en-1-yloxy)pentanoic acid Fmoc-L-glutamic acid |A-allyl ester L-Fmoc-Glu-OAll Fmoc-Glu-OAllyl Nα-(9-fluorenylmethoxycbonyl)-L-glutamic acid α-allyl ester N-Fluorene methoxycbonyl-L-Glutamate-1-allyl ester L-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1-(2-propen-1-yl) ester FMOC-GLU(OME)-OH N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamic Acid 1-Allyl Ester MFCD00467718 N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-GLUTAMIC ACID ALPHA-ALLYL ESTER FMOC-GLU-OALLFMOC-GL N-ALPHA-(9-FLUORENYLMETHYLOXYCBONYL)-L-GLUTAMIC-ACID-ALPHA ALLYL ESTER FMOC-GLU-OAL FMOC-GLUTAMIC ACID-ALLYL ESTER 1-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate FMOC-L-GLU-OALL N-ALPHA-FMOC-L-GLUTAMIC ACID ALPHA-ALLYL ESTER 1-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate > FMOC-L-GLUTAMIC ACID ALPHA-ALLYL ESTER Fmoc-Glu-OAll FMOC-GLU-OALL FMOC-GLU-OALL ISO 9001:2015 REACH FMOC-L-GLUTAMIC ACID ALPHA-AL FMOC-GLU-ALLYL ESTER (S)-4-((((9H-Fluoren-9-yl)Methoxy)carbonyl)amino)-5-(allyloxy)-5-oxopentanoic acid FMOC-L-GLUTAMIC ACID 1-ALLYL ESTER (4S)-5-allyloxy-4-(9H-fluoren-9-ylmethoxycbonylamino)-5-oxo-pentanoic acid FMOC-GLU-OALL;FMOC-L-GLUTAMIC ACID 1-ALLYL ESTER;FMOC-L-GLUTAMIC ACID ALPHA-ALLYL ESTER; ESTER;FMOC-GLU-OAL;FMOC-GLU-OALL;FMOC-GLU-ALLYL ESTER;N-ALPHA-(9-FLUORENYLMETHYLOXYCBONYL)-L-GLUTAMIC-ACID-ALPHA ALLYL ESTER N-Fmoc-L-glutamic acid 1-allyl ester (9H-Fluoren-9-yl)MethOxy]carbonyl Glu-OAll (4S)-4-(9H-fluoren-9-ylmethoxycbonylamino)-5-oxo-5-prop-2-enoxypentanoic acid 1-Allyl N-Fmoc-L-glutamate Fmoc-L-glutamic acid 1-allyl ester 3-chloro-1-(3,4-dichlorophenyl)-4-(morpholin-4-yl)-1H-pyrrole-2,5-dione |
| Description | Fmoc-Glu-OAll is a glutamic 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 | 1.264g/cm3 |
|---|---|
| Boiling Point | 652.3ºC at 760 mmHg |
| Melting Point | 118-122ºC |
| Molecular Formula | C23H23NO6 |
| Molecular Weight | 409.43200 |
| Flash Point | 348.3ºC |
| Exact Mass | 409.15300 |
| PSA | 101.93000 |
| LogP | 3.87860 |
| Vapour Pressure | 6.64E-18mmHg at 25°C |
| Index of Refraction | 1.585 |
| Storage condition | 2-8°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Safety Phrases | S22 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2924299090 |
|
~88%
144120-54-7 |
| Literature: Nuijens, Timo; Cusan, Claudia; Kruijtzer, John A. W.; Rijkers, Dirk T. S.; Liskamp, Rob M. J.; Quaedflieg, Peter J. L. M. Synthesis, 2009 , # 5 p. 809 - 814 |
|
~%
144120-54-7 |
| Literature: Tetrahedron Letters, , vol. 34, # 10 p. 1549 - 1552 |
| Precursor 3 | |
|---|---|
| DownStream 0 | |
| HS Code | 2924299090 |
|---|---|
| Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |