
CAS Number199006-54-7
Synonyms(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-methylphenyl)propanoic acid; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-methyl-L-phenylalanine; Fmoc-Phe(4-Me)-OH; (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-(4-methylphenyl)propanoic acid; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(p-tolyl)propanoic acid; Fmoc-D-phe(4-me)-OH; Fmoc-L-4-Methylphe; MFCD00270197
Molecular FormulaC25H23NO4
Molecular Weight401.46
Density1.3±0.1 g/cm3
Boiling Point629.1±55.0 °C at 760 mmHg
Melting Point168ºC
AppearanceSolid;White to Almost white powder to crystal
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 199006-54-7 |
| Catalog No. | 2A-9078105 |
| Chinese Name | Fmoc-L-4-甲基苯丙氨酸 |
| Synonyms | (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-methylphenyl)propanoic acid; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-methyl-L-phenylalanine; Fmoc-Phe(4-Me)-OH; (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-(4-methylphenyl)propanoic acid; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(p-tolyl)propanoic acid; Fmoc-D-phe(4-me)-OH; Fmoc-L-4-Methylphe; MFCD00270197 |
| Molecular Formula | C25H23NO4 |
| Molecular Weight | 401.46 |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 629.1±55.0 °C at 760 mmHg |
| Melting Point | 168ºC |
| Appearance | Solid;White to Almost white powder to crystal |
| Water Solubility | Soluble in: dimethylformamide |
| Storage Condition | 0-10°C; avoid heating |
| Application | Fmoc-Phe(4-Me)-OH is a phenylalanine derivative [1]. |
| HTC | 2924299090 |
| PubChem ID | 16417127 |
| SMILES | Cc1ccc(CC(NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)O)cc1 |
| InChI | InChI=1S/C25H23NO4/c1-16-10-12-17(13-11-16)14-23(24(27)28)26-25(29)30-15-22-20-8-4-2-6-18(20)19-7-3-5-9-21(19)22/h2-13,22-23H,14-15H2,1H3,(H,26,29)(H,27,28)/t23-/m0/s1 |
| InChI Key | UXLHLZHGQPDMJQ-QHCPKHFHSA-N |
| Use of | Fmoc-Phe(4-Me)-OH is a phenylalanine derivative[1]. Properties Name Fmoc-4-methyl-L-phenylalanine Synonym More Synonyms Fmoc-Phe(4-Me)-OH Biological Activity Description Fmoc-Phe(4-Me)-OH is a phenylalanine derivative[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others 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 [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-843. Chemical & Physical Properties Molecular Formula C25H23NO4 Exact Mass 401.162720 PSA 75.63000 Index of Refraction 1.626 InChIKey UXLHLZHGQPDMJQ-QHCPKHFHSA-N Safety Information Hazard Codes Xi WGK Germany 3 HS Code 2924299090 |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Product name: 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% |
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