CAS Number90600-20-7
Synonyms(S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pent-4-enoic acid; (2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-4-pentenoic acid; Boc-L-Allylglycine; (S)-N-Boc-allylglycine; MFCD01320851
Molecular FormulaC10H17O4N1
Molecular Weight215.25
Density1.1±0.1 g/cm3
Boiling Point352.0±35.0 °C at 760 mmHg
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 90600-20-7 |
| Catalog No. | 2A-9082299 |
| Chinese Name | Boc-L-烯丙基甘氨酸 |
| Synonyms | (S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pent-4-enoic acid; (2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-4-pentenoic acid; Boc-L-Allylglycine; (S)-N-Boc-allylglycine; MFCD01320851 |
| Molecular Formula | C10H17O4N1 |
| Molecular Weight | 215.25 |
| Density | 1.1±0.1 g/cm3 |
| Boiling Point | 352.0±35.0 °C at 760 mmHg |
| Storage Condition | Sealed in a cool, dry environment |
| Application | (S)-2-((tert-butoxycarbonyl)amino)pent-4-enoic acid is a derivative of glycine (HY-Y0966) [1]. |
| HTC | 2924199090 |
| MDL Number | MFCD01320851 |
| SMILES | C=CCC(NC(=O)OC(C)(C)C)C(=O)O |
| InChI | InChI=1S/C10H17NO4/c1-5-6-7(8(12)13)11-9(14)15-10(2,3)4/h5,7H,1,6H2,2-4H3,(H,11,14)(H,12,13)/p-1/t7-/m0/s1 |
| InChI Key | BUPDPLXLAKNJMI-ZETCQYMHSA-N |
| MSDS | msds/82299_1_90600_20_7.pdf |
| Bioactivity | (S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid 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 1.1±0.1 g/cm3 Boiling Point 352.0±35.0 °C at 760 mmHg Molecular Formula C10H17NO4 Molecular Weight 215.246 Flash Point 166.7±25.9 °C Exact Mass 215.115753 PSA 66.84000 LogP 2.04 Vapour Pressure 0.0±1.7 mmHg at 25°C Index of Refraction 1.473 InChIKey BUPDPLXLAKNJMI-ZETCQYMHSA-N SMILES C=CCC(NC(=O)OC(C)(C)C)C(=O)O Storage condition 2-8°C |
| Use of | (S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid is a Glycine (HY-Y0966) derivative[1]. Properties Name (S)-N-BOC-Allylglycine Synonym More Synonyms Boc-L-Allylglycine Biological Activity Description (S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid 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 C10H17NO4 Exact Mass 215.115753 PSA 66.84000 Index of Refraction 1.473 InChIKey BUPDPLXLAKNJMI-ZETCQYMHSA-N SMILES C=CCC(NC(=O)OC(C)(C)C)C(=O)O |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Product name: Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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