104091-08-9
104091-08-9 structure
- Name: Fmoc-D-Glu(OtBu)-OH
- Chemical Name: N-Alpha-Fmoc-D-Glutamic Acid Gamma-T-Butyl Ester
- CAS Number: 104091-08-9
- Molecular Formula: C24H27NO6
- Molecular Weight: 425.474
- Catalog: Biochemical Amino acids and their derivatives Glutamic acid derivative
- Create Date: 2018-10-09 11:54:35
- Modify Date: 2026-07-01 16:33:49
-
Fmoc-D-Glu(OtBu)-OH is a glutamic acid derivative[1].
| Name | N-Alpha-Fmoc-D-Glutamic Acid Gamma-T-Butyl Ester |
|---|---|
| Synonyms |
N-fluorene methoxycbonyl-D-glutamic acid-5-tert-butyl ester
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-glutamic Acid 5-tert-Butyl Ester N-ALPHA-FMOC-D-GLUTAMIC ACID GAMMA-TERT-BUTYL ESTER Fmoc-L-Histidine(Trt)-OH (9H-Fluoren-9-yl)MethOxy]carbonyl D-Glu(OtBu)-OH FMOC-D-GLU(OBUT)-OH N-(9-Fluorenylmethoxycbonyl)-D-glutamic acid 5-tert-butyl ester n-(9-fluorenylmethoxycbonyl)-d-glutamic acid gamma-tert-butyl ester Fmoc- D -Glu(OtBu)-OH L-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 5-(1,1-dimethylethyl) ester FMOC-D-GLU(OTBU)-OH FMOC-D-GLUTAMIC ACID(OTBU)-OH Fmoc-D-glutamicacid1-tert·butylester Fmoc-D-Glutamic acid 5-tert-butyl ester (R)-2-((((9H-fluoren-9-yl)Methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid Fmoc-D-Glutamate-5-tert-butyl ester FMOC-D-GLU(TBU)-OH H2O N-α-Fmoc-L-glutamic acid γ-t.-butyl ester monohydrate (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-5-[(2-methyl-2-propanyl)oxy]-5-oxopentanoic acid amma-tert-butyL (2S)-5-tert-Butoxy-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-5-oxopentanoic acid (non-preferred name) FMOC-D-GLUTAMIC ACID 5-TERT-BUTYL ESTER N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-D-GLUTAMIC ACID GAMMA-T-BUTYL ESTER MONOHYDRATE N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-glutamic Acid 5-tert-Butyl Ester Fmoc-D-Glu(OtBu)-OH 5-tert-Butyl N-Fmoc-D-glutamate Fmoc-Glu(OtBu)-OH N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-D-GLUTAMIC ACID GAMMA-T-BUTYL ESTER Fmoc-D-glutamic acid gamma-tert-butyl ester //BP Fmoc-D-glutamic acid γ-tert-butyl ester (HPLC) (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-[(2-methylpropan-2-yl)oxy]-5-oxopentanoic acid 9-FLUORENYLMETHOXYCBONYL-D-GLUTAMIC ACID GAMMA-T-BUTYL ESTER MONOHYDRATE (2R)-5-tert-Butoxy-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-5-oxopentanoic acid (non-preferred name) 5-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-glutamate quinolin-6-cbaldehyde utamic acid g 5-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-glutamate Hydrate NALPHA-9-Fluorenylmethoxycbonyl-D-glutamic acid GAMMA-tert-butyl ester (2R)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-5-[(2-methyl-2-propanyl)oxy]-5-oxopentanoic acid N-fluorene methoxycbonyl d-glutamate-gamma-tert-butyl ester 5-tert-Butyl N-Fmoc-D-glutamate Hydrate N-Fmoc-D-glutamic acid 5-tert-butyl ester N-ALPHA-FMOC-D-GLUTAMIC ACID GAMMA-T-BUTYL ESTER Fmoc-D-g FMOC-D-GLUTAMIC ACID .GAMMA.-TERT-BUTYLESTER MONOHYDRATE 5-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-glutamate Hydrate> FMOC-D-GLUTAMIC ACID(O-T-BUTYL) FMOC-D-GLU(OBUT) H2O N-ALPHA-(9-FLUORENYLMETHYLOXYCBONYL)-D-GLUTAMIC-ACID-GAMMA-T-BUTYL ESTER Fmoc-D-glutamic acid gamma-tert-butyl ester N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-glutamic Acid 5-tert-Butyl Ester Hydrate FMOC-D-GLU(OTBU)-OH H2O N-α-fmoc-D-glutamic acid-γ-tert-butyl ester Fmoc-D-Glu(OtBu)-OH Hydrate Fmoc-Glu(OBut)-OH·H2O 6-FmocQUINOLINE FMOC-D-GLUTAMIC ACID GAMMA-T-BUTYL ESTER D-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 5-(1,1-dimethylethyl) ester FMoc-D-Glu(OBut) FMOC-D-Glutamic Acid 5-Tert-Butyl Ester (FMOC-D-Glu(OtBu)-OH) extrapure N-ALPHA-(9-FLUORENYLMETHYLOXYCBONYL)-D-GLUTAMIC-ACID-GAMMA-TERT-BUTYL ESTER MONOHYDRATE MFCD00797526 N-alpha-(9-Fluorenylmethyloxycbonyl)-D-glutamic-acid-gamma-t-butyl ester monohydrate 5-tert-Butyl N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-D-glutaMate Hydrate FMOC-D-GLU(TBU)-OH Fmoc-D-gL Fmoc-D-Glu(OtBu)-OH >= (HPLC) 5-tert-Butyl N-Fmoc-D-glutamate utamic acid gamma-tert-butyL (2R)-5-(tert-butoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-5-oxopentanoic acid |
| Description | Fmoc-D-Glu(OtBu)-OH 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 | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 633.5±55.0 °C at 760 mmHg |
| Melting Point | 83-89ºC |
| Molecular Formula | C24H27NO6 |
| Molecular Weight | 425.474 |
| Flash Point | 337.0±31.5 °C |
| Exact Mass | 425.183838 |
| PSA | 101.93000 |
| LogP | 5.26 |
| Vapour Pressure | 0.0±2.0 mmHg at 25°C |
| Index of Refraction | 1.571 |
| Storage condition | 2-8°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
|
~98%
104091-08-9 |
| Literature: Journal of Organic Chemistry, , vol. 51, # 24 p. 4590 - 4594 |
|
~72%
104091-08-9 |
| Literature: Journal of Organic Chemistry, , vol. 51, # 24 p. 4590 - 4594 |
|
~%
104091-08-9 |
| Literature: Journal of Organic Chemistry, , vol. 51, # 24 p. 4590 - 4594 |
|
~%
104091-08-9 |
| Literature: Journal of Organic Chemistry, , vol. 51, # 24 p. 4590 - 4594 |
| Precursor 5 | |
|---|---|
| DownStream 1 | |
