CAS Number170642-28-1
Synonyms(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-pentenoic acid; (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pent-4-enoic acid; MFCD01311776; Fmoc-D-allyl-Gly-OH; 2-Allyl-N-Fmoc-D-glycine; N-Allyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycine; Fmoc-D-Gly(allyl)-OH; (R)-N-Fmoc-Allylglycine; (R)-N-Fmoc-allyl-glycine; Fmoc-D-Allylglycine
Molecular FormulaC20H19NO4
Molecular Weight337.38
Purity96+%
Density1.3±0.1 g/cm3
Boiling Point531.6±39.0 °C at 760 mmHg
Melting Point134 °C
Appearancewhite granular powder
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 170642-28-1 |
| Catalog No. | 2A-0099481 |
| Chinese Name | Fmoc-D-烯丙基甘氨酸 |
| Synonyms | (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-pentenoic acid; (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pent-4-enoic acid; MFCD01311776; Fmoc-D-allyl-Gly-OH; 2-Allyl-N-Fmoc-D-glycine; N-Allyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycine; Fmoc-D-Gly(allyl)-OH; (R)-N-Fmoc-Allylglycine; (R)-N-Fmoc-allyl-glycine; Fmoc-D-Allylglycine |
| Molecular Formula | C20H19NO4 |
| Molecular Weight | 337.38 |
| Purity | 96+ |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 531.6±39.0 °C at 760 mmHg |
| Melting Point | 134 °C |
| Appearance | white granular powder |
| Storage Condition | Sealed in a cool, dry environment at 0 ºC |
| Application | Fmoc-D-Gly(allyl)-OH is a derivative of glycine (HY-Y0966) [1]. |
| EINECS | 0 |
| HTC | 0 |
| UN(IATA) | 0 |
| SMILES | C=CCC(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O |
| InChI | InChI=1S/C20H19NO4/c1-2-7-18(19(22)23)21-20(24)25-12-17-15-10-5-3-8-13(15)14-9-4-6-11-16(14)17/h2-6,8-11,17-18H,1,7,12H2,(H,21,24)(H,22,23)/p-1/t18-/m1/s1 |
| InChI Key | YVBLQCANYSFEBN-GOSISDBHSA-N |
| Bioactivity | Fmoc-D-Gly(allyl)-OH is a Glycine (HY-Y0966) 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 531.6±39.0 °C at 760 mmHg Melting Point 134 °C Molecular Formula C20H19NO4 Molecular Weight 337.369 Flash Point 275.3±27.1 °C Exact Mass 337.131409 PSA 66.84000 LogP 4.54 Vapour Pressure 0.0±1.5 mmHg at 25°C Index of Refraction 1.609 InChIKey YVBLQCANYSFEBN-GOSISDBHSA-N SMILES C=CCC(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O Storage condition Store at 0°C |
| Use of | Fmoc-D-Gly(allyl)-OH is a Glycine (HY-Y0966) derivative[1]. Properties Name (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pent-4-enoic acid Synonym More Synonyms (R)-N-Fmoc-Allylglycine Biological Activity Description Fmoc-D-Gly(allyl)-OH is a Glycine (HY-Y0966) 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 C20H19NO4 Exact Mass 337.131409 PSA 66.84000 Index of Refraction 1.609 InChIKey YVBLQCANYSFEBN-GOSISDBHSA-N |
| Transport Info | Product name: Fmoc-D-allylglycine |
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