| Name | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pent-4-enoic acid |
|---|---|
| Synonyms |
N-Fmoc-allyl-L-glycine
4-Pentenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2S) 2-Allyl-N-Fmoc-L-glycine (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pent-4-enoic acid Fmoc-allyl-L-glycine (S)-N-FMOC-Allylglycine, ee (S)-FMOC-ALLYLGLYCINE (S)-2-(FMOC-AMINO)-4-PENTENOIC ACID Fmoc-L-Allylglycine Fmoc-allyl-L-glycine (HPLC, Chiral purity) (S)-N-FMOC-ALLYLGLYCINE EE Fmoc-Allyglycine 2-[[9H-fluoren-9-ylmethoxy(oxo)methyl]-prop-2-enylamino]acetic acid FMOC-ALLYL-L-GLYCINE (S)-2-(Fmoc-amino)-4-pentenoic acid, Fmoc-L-2-allylglycine Fmoc-L-Gly(allyl)-OH RECHEM BK PT 0251 N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-ALPHA-ALLYL-GLYCINE (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pent-4-e N-FMOC protected FMOC-L-2-ALLYLGLYCINE L-2-Allylglycine, N-FMOC protected Fmoc-L-2-allylglycine Fmoc-L-Alpha-Allyl-Gly (9H-Fluoren-9-yl)MethOxy]carbonyl L-Gly(Allyl)-OH FMoc-(S)-2-Allylglycine FMOC-L-2-allylglycine Hydrochloride (S)-N-Fmoc-Allylglycine //BP FMOC-(S)-2-AMINO-4-PENTENOIC ACID S3-NM Fmoc-L-Allylglycine CAS FMoc-L-Allyglycine FMoc-L-Allyglycine (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pent-4-enoicaci (S)-N-fmoc-Allylglycine(e.e.) Fmoc-Gly(Allyl)-OH FMOC-(ALLYL)GLY-OH (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-pentenoic acid FMOC-ALGLY-OH (S)-2-FMoc-amino-4-pentenoic acid, FMoc-L-allylglycine FMOC-ALPHA-ALLYL-L-GLY FMoc-a-allyl-Gly-OH (S)-N-FMOC-ALLYLGLYCINE Fmoc-L-ALG Fmoc-allyl-Gly-OH (2S)-2-(9H-fluoren-9-ylmethoxycbonylamino)pent-4-enoic acid FMOC-GLY(ALLYL)-OH N-Fluorenemethoxycbonyl-L-Allyl Glycine Fmoc-L-Allyglycine Fmoc-2-allyl-L-glycine FMOC-L-ALLYLGLYCINE (S)-2-(((9H-fluoren-9-yl)Methoxy)cbonylaMino)pent-4-enoic acid MFCD01311749 (S)-N-(9-FLUORENYLMETHOXYCBONYL)-2-AMINO-4-PENTENOIC ACID |
| Description | Fmoc-Gly(allyl)-OH is a Glycine (HY-Y0966) 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 | 563.0±45.0 °C at 760 mmHg |
| Melting Point | 137.1ºC |
| Molecular Formula | C20H19NO4 |
| Molecular Weight | 337.369 |
| Flash Point | 294.3±28.7 °C |
| Exact Mass | 337.131409 |
| PSA | 75.63000 |
| LogP | 4.48 |
| Vapour Pressure | 0.0±1.6 mmHg at 25°C |
| Index of Refraction | 1.602 |
| Storage condition | 2-8°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Safety Phrases | S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2922509090 |
|
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| Literature: Besada, Pedro; Mamedova, Liaman; Thomas, Craig J.; Costanzi, Stefano; Jacobson, Kenneth A. Organic and Biomolecular Chemistry, 2005 , vol. 3, # 10 p. 2016 - 2025 |
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| Literature: Oppolzer, Wolfgang; Lienard, Philippe Helvetica Chimica Acta, 1992 , vol. 75, # 8 p. 2572 - 2582 |
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| Literature: European Journal of Medicinal Chemistry, , vol. 69, p. 232 - 243 |
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| Literature: Organic Letters, , vol. 6, # 19 p. 3285 - 3288 |
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| Literature: Helvetica Chimica Acta, , vol. 75, # 8 p. 2572 - 2582 |
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| Literature: Helvetica Chimica Acta, , vol. 75, # 8 p. 2572 - 2582 |
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| Literature: Helvetica Chimica Acta, , vol. 75, # 8 p. 2572 - 2582 |
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| Literature: Chemical Communications, , vol. 49, # 71 p. 7840 - 7841 |
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| Literature: Journal of Organic Chemistry, , vol. 70, # 10 p. 3838 - 3844 |
| Precursor 7 | |
|---|---|
| DownStream 4 | |
| HS Code | 2922509090 |
|---|---|
| Summary | 2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |