CAS Number86060-92-6
SynonymsFmoc-phenylalanine pentafluorophenyl ester; Fmoc-Phe-OPfp; N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine pentafluorophenyl ester; Fmoc-Phe pentafluorophenyl ester; Fmoc-L-Phe-OPfp; Fmoc-L-phenylalanine pentafluorophenyl ester; Fmoc-D-Phe-OPfp; Fmoc-Phe-OC6F5; MFCD00065669
Molecular FormulaC30H20F5NO4
Molecular Weight553.48
Purity96+%
Density1.399g/cm3
Boiling Point674.8ºC at 760 mmHg
Melting Point149-151 °C(lit.)
Appearancewhite crystal
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 86060-92-6 |
| Catalog No. | 2A-0155859 |
| Chinese Name | N-芴甲氧羰基-L-苯丙氨酸五氟苯酯 |
| Synonyms | Fmoc-phenylalanine pentafluorophenyl ester; Fmoc-Phe-OPfp; N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine pentafluorophenyl ester; Fmoc-Phe pentafluorophenyl ester; Fmoc-L-Phe-OPfp; Fmoc-L-phenylalanine pentafluorophenyl ester; Fmoc-D-Phe-OPfp; Fmoc-Phe-OC6F5; MFCD00065669 |
| Molecular Formula | C30H20F5NO4 |
| Molecular Weight | 553.48 |
| Purity | 96+ |
| Density | 1.399g/cm3 |
| Boiling Point | 674.8ºC at 760 mmHg |
| Melting Point | 149-151 °C(lit.) |
| Appearance | white crystal |
| Storage Condition | Refrigerated, airtight, dry place at 2-8°C |
| Application | Fmoc-Phe OPfp is a phenylalanine derivative [1]. |
| EINECS | 0 |
| HTC | 0 |
| UN(IATA) | 0 |
| PubChem ID | 3152465 |
| MDL Number | MFCD00065669 |
| SMILES | O=C(NC(Cc1ccccc1)C(=O)Oc1c(F)c(F)c(F)c(F)c1F)OCC1c2ccccc2-c2ccccc21 |
| InChI | InChI=1S/C30H20F5NO4/c31-23-24(32)26(34)28(27(35)25(23)33)40-29(37)22(14-16-8-2-1-3-9-16)36-30(38)39-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,36,38)/t22-/m0/s1 |
| InChI Key | WKHPSOMXNCTXPK-QFIPXVFZSA-N |
| NACRES Code | NA.22 |
| UNSPSC | 12352209 |
| Bioactivity | Fmoc-Phe-OPfp 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):1793-938. Chemical & Physical Properties Density 1.399g/cm3 Boiling Point 674.8ºC at 760 mmHg Melting Point 149-151 °C(lit.) Molecular Formula C30H20F5NO4 Molecular Weight 553.47600 Flash Point 361.9ºC Exact Mass 553.13100 PSA 64.63000 LogP 6.82840 Index of Refraction 1.588 InChIKey WKHPSOMXNCTXPK-QFIPXVFZSA-N SMILES O=C(NC(Cc1ccccc1)C(=O)Oc1c(F)c(F)c(F)c(F)c1F)OCC1c2ccccc2-c2ccccc21 Storage condition 2-8°C |
| Use of | Fmoc-Phe-OPfp is a phenylalanine derivative[1]. Properties Name (2,3,4,5,6-pentafluorophenyl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenylpropanoate Synonym More Synonyms Fmoc-Phe-OPfp Biological Activity Description Fmoc-Phe-OPfp 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):1793-938. Chemical & Physical Properties Molecular Formula C30H20F5NO4 Exact Mass 553.13100 PSA 64.63000 LogP 6.82840 Index of Refraction 1.588 InChIKey WKHPSOMXNCTXPK-QFIPXVFZSA-N |
| Transport Info | Product name: FMOC-L-phenylalanine pentafluorophenyl ester |
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