CAS Number146982-24-3
SynonymsFmoc-Asp(OAll)-OH; (S)-3-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(allyloxy)-4-oxobutanoic acid; FMoc-Asp; FMOC-L-ASP-OALL; Fmoc-L-Asp(OAll)-OH; FMOC-ASP-ALLYL ESTER; Fmoc-L-Asp(OH)OAll; FMOC-ASP-OAI; Fmoc-Asp-Oal; FMOC-L-ASPARTIC ACID-B-ALLYLESTER; L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(2-propen-1-yl) ester; Fmoc-L-aspartic acid 1-allyl ester; (2S)-4-(Allyloxy)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid; Fmoc-L-aspartic acid 4-allyl ester; Fmoc-L-Aspartic acid alpha-allyl ester; Fmoc-Asp-OAll; L-Fmoc-Asp-OAll; N-[(9H-Fluoren-9-ylmethyloxycarbonyl)]-L-aspartic Acid 1-Allyl Ester; N-Fmoc-L-aspartic Acid 1-Allyl Ester; (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(allyloxy)-4-oxobutanoic acid; 1-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-as
Molecular FormulaC22H21NO6
Molecular Weight395.41
Purity96+%
Density1.3±0.1 g/cm3
Boiling Point638.5±55.0 °C at 760 mmHg
Melting Point111-115ºC
AppearanceWhite to off-white free flowing powder
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 146982-24-3 |
| Catalog No. | 2A-0155645 |
| Chinese Name | N-芴甲氧羰基-L-天冬氨酸 4-烯丙酯 |
| Synonyms | Fmoc-Asp(OAll)-OH; (S)-3-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(allyloxy)-4-oxobutanoic acid; FMoc-Asp; FMOC-L-ASP-OALL; Fmoc-L-Asp(OAll)-OH; FMOC-ASP-ALLYL ESTER; Fmoc-L-Asp(OH)OAll; FMOC-ASP-OAI; Fmoc-Asp-Oal; FMOC-L-ASPARTIC ACID-B-ALLYLESTER; L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(2-propen-1-yl) ester; Fmoc-L-aspartic acid 1-allyl ester; (2S)-4-(Allyloxy)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid; Fmoc-L-aspartic acid 4-allyl ester; Fmoc-L-Aspartic acid alpha-allyl ester; Fmoc-Asp-OAll; L-Fmoc-Asp-OAll; N-[(9H-Fluoren-9-ylmethyloxycarbonyl)]-L-aspartic Acid 1-Allyl Ester; N-Fmoc-L-aspartic Acid 1-Allyl Ester; (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(allyloxy)-4-oxobutanoic acid; 1-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-as |
| Molecular Formula | C22H21NO6 |
| Molecular Weight | 395.41 |
| Purity | 96+ |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 638.5±55.0 °C at 760 mmHg |
| Melting Point | 111-115ºC |
| Appearance | White to off-white free flowing powder |
| Storage Condition | 2-8°C |
| Application | Fmoc-Asp(OAll)-OH is an aspartic acid derivative [1]. |
| EINECS | 0 |
| HTC | 0 |
| UN(IATA) | 0 |
| PubChem ID | 15750850 |
| SMILES | C=CCOC(=O)CC(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O |
| InChI | InChI=1S/C22H21NO6/c1-2-11-28-20(24)12-19(21(25)26)23-22(27)29-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h2-10,18-19H,1,11-13H2,(H,23,27)(H,25,26)/t19-/m0/s1 |
| InChI Key | FBNFRRNBFASDKS-IBGZPJMESA-N |
| Bioactivity | Fmoc-Asp(OAll)-OH 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 638.5±55.0 °C at 760 mmHg Melting Point 111-115ºC Molecular Formula C22H21NO6 Molecular Weight 395.405 Flash Point 340.0±31.5 °C Exact Mass 395.136902 PSA 101.93000 LogP 4.75 Vapour Pressure 0.0±2.0 mmHg at 25°C Index of Refraction 1.592 InChIKey FBNFRRNBFASDKS-IBGZPJMESA-N SMILES C=CCOC(=O)CC(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O Storage condition 2-8°C |
| Use of | Fmoc-Asp(OAll)-OH is an aspartic acid derivative[1]. Properties Name Fmoc-L-Aspartic acid β-allyl ester Synonym More Synonyms Fmoc-Asp(OAll)-OH Biological Activity Description Fmoc-Asp(OAll)-OH 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 C22H21NO6 Exact Mass 395.136902 PSA 101.93000 Index of Refraction 1.592 InChIKey FBNFRRNBFASDKS-IBGZPJMESA-N |
| Transport Info | Product name: Fmoc-L-aspartic acid 4-allyl ester |
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