CAS Number201481-37-0
Synonyms(2S,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid; AmbotzFAA1655; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-O-(2-methyl-2-propanyl)-L-allothreonine; Fmoc-Allo-Thr(tBu)-OH
Molecular FormulaC23H27O5N1
Molecular Weight397.47
Purity96+%
Density1.2±0.1 g/cm3
Boiling Point581.7±50.0 °C at 760 mmHg
AppearanceSolid | White
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 201481-37-0 |
| Catalog No. | 2A-0155632 |
| Chinese Name | N-芴甲氧羰基-L- 别苏氨酸叔丁醚 |
| Synonyms | (2S,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid; AmbotzFAA1655; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-O-(2-methyl-2-propanyl)-L-allothreonine; Fmoc-Allo-Thr(tBu)-OH |
| Molecular Formula | C23H27O5N1 |
| Molecular Weight | 397.47 |
| Purity | 96+ |
| Density | 1.2±0.1 g/cm3 |
| Boiling Point | 581.7±50.0 °C at 760 mmHg |
| Appearance | Solid | White |
| Storage Condition | Storage method: 2 -8 °C |
| Application | O-(tert-butyl)-N-Fmoc-L-isothreonine is a threonine derivative [1]. |
| EINECS | 0 |
| HTC | 0 |
| UN(IATA) | 0 |
| PubChem ID | 8788070 |
| MDL Number | MFCD00237371 |
| SMILES | CC(OC(C)(C)C)C(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O |
| InChI | InChI=1S/C23H27NO5/c1-14(29-23(2,3)4)20(21(25)26)24-22(27)28-13-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h5-12,14,19-20H,13H2,1-4H3,(H,24,27)(H,25,26)/t14-,20-/m0/s1 |
| InChI Key | LZOLWEQBVPVDPR-XOBRGWDASA-N |
| Bioactivity | O-(tert-Butyl)-N-Fmoc-L-allothreonine is a threonine 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 1.2±0.1 g/cm3 Boiling Point 581.7±50.0 °C at 760 mmHg Molecular Formula C23H27NO5 Molecular Weight 397.464 Flash Point 305.6±30.1 °C Exact Mass 397.188934 PSA 84.86000 LogP 5.45 Appearance of Characters Solid | White Vapour Pressure 0.0±1.7 mmHg at 25°C Index of Refraction 1.569 InChIKey LZOLWEQBVPVDPR-XOBRGWDASA-N SMILES CC(OC(C)(C)C)C(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O Storage condition 2-8°C |
| Use of | O-(tert-Butyl)-N-Fmoc-L-allothreonine is a threonine derivative[1]. Properties Name (2S,3S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxy]butanoic acid Synonym More Synonyms Fmoc-Allo-Thr(tBu)-OH Biological Activity Description O-(tert-Butyl)-N-Fmoc-L-allothreonine is a threonine 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 C23H27NO5 Exact Mass 397.188934 PSA 84.86000 Appearance of Characters Solid | White Index of Refraction 1.569 InChIKey LZOLWEQBVPVDPR-XOBRGWDASA-N |
| Transport Info | Product name: N-Fmoc-O-tert-butyl-L-allo-threonine |
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