CAS Number145038-53-5
SynonymsFmoc-L-Aspartic acid 4-methyl ester; (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-methoxy-4-oxobutanoic acid; Fmoc-L-Asp(OMe)-OH; Fmoc-Asp(OMe)-OH; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methoxy-4-oxobutanoic acid; Fmoc-Aspartic acid 4-methyl ester; L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-methyl ester
Molecular FormulaC20H19O6N1
Molecular Weight369.37
Purity96+%
Density1.3±0.1 g/cm3
Boiling Point613.7±55.0 °C at 760 mmHg
AppearanceSolid
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 145038-53-5 |
| Catalog No. | 2A-0155654 |
| Chinese Name | Fmoc-L-天冬氨酸4-甲酯 |
| Synonyms | Fmoc-L-Aspartic acid 4-methyl ester; (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-methoxy-4-oxobutanoic acid; Fmoc-L-Asp(OMe)-OH; Fmoc-Asp(OMe)-OH; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methoxy-4-oxobutanoic acid; Fmoc-Aspartic acid 4-methyl ester; L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-methyl ester |
| Molecular Formula | C20H19O6N1 |
| Molecular Weight | 369.37 |
| Purity | 96+ |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 613.7±55.0 °C at 760 mmHg |
| Appearance | Solid |
| Storage Condition | 2-8°C |
| Application | N-9-fluorobenzyloxycarbonylpropionic acid β-methyl ester is an aspartic acid derivative [1]. |
| EINECS | 0 |
| HTC | 0 |
| UN(IATA) | 0 |
| PubChem ID | 93374719 |
| MDL Number | MFCD08458573 |
| InChI | InChI=1S/C20H19NO6/c1-26-18(22)10-17(19(23)24)21-20(25)27-11-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,16-17H,10-11H2,1H3,(H,21,25)(H,23,24)/t17-/m0/s1 |
| InChI Key | HSOKCYGOTGVDHL-KRWDZBQOSA-N |
| Bioactivity | N-9-Fluorenylmethoxycarbonylaspartic acid β-methyl ester is an aspartic acid 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):1793-1144. Chemical & Physical Properties Density 1.3±0.1 g/cm3 Boiling Point 613.7±55.0 °C at 760 mmHg Molecular Formula C20H19NO6 Molecular Weight 369.368 Flash Point 325.0±31.5 °C Exact Mass 369.121246 PSA 101.93000 LogP 3.93 Appearance of Characters Solid Vapour Pressure 0.0±1.9 mmHg at 25°C Index of Refraction 1.596 Storage condition 2-8°C |
| Use of | N-9-Fluorenylmethoxycarbonylaspartic acid β-methyl ester is an aspartic acid derivative[1]. Properties Name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methoxy-4-oxobutanoic acid Synonym More Synonyms Fmoc-Asp(OMe)-OH Biological Activity Description N-9-Fluorenylmethoxycarbonylaspartic acid β-methyl ester is an aspartic acid 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):1793-1144. Chemical & Physical Properties Molecular Formula C20H19NO6 Exact Mass 369.121246 PSA 101.93000 Appearance of Characters Solid Index of Refraction 1.596 |
| Transport Info | Product name: Fmoc-L-aspartic acid 4-methyl ester |
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