CAS Number18942-49-9
SynonymsBoc-D-Phe-OH; (2R)-2-[(tert-butoxy)carbonylamino]-3-phenylpropanoic acid; N-(t-butyloxycarbonyl)-D-Phenylalanine; Boc-phenylalanine; BOC-D-PHE; Boc-L-Phenylalanine; (2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoic acid; N-Boc-D-phenylalanine; (S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropanoic acid; N-(tert-Butoxycarbonyl)-L-phenylalanine; boc-L-Phe; MFCD00063149; N-t-Butyloxycarbonyl-L-phenylalanine; N-α-t-BOC-L-phenylalanine; N-(t-Butyloxycarbonyl)-R-phenylalanine; (R)-N-(tert-butoxycarbonyl)phenylalanine; N-tert-Butyloxycarbonyl-L-phenylalanine; Boc-D-phenylalanine; N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-phenylalanine; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid; N-(tert-butoxycarbonyl)-D-phenylalanine; N-(tert-Butoxycarbonyl)-L-phenylala
Molecular FormulaC14H19NO4
Molecular Weight265.30
Purity≥99.0 (sum of enantiomers, TLC)%
Density1.2±0.1 g/cm3
Boiling Point426.6±38.0 °C at 760 mmHg
Melting Point85-88ºC
AppearanceWhite to off-white crystalline powder
Symbol
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| Chemical & Physical Properties | |
|---|---|
| CAS Number | 18942-49-9 |
| Catalog No. | 2A-0201757 |
| Chinese Name | N-BOC-D-苯丙氨酸 |
| Synonyms | Boc-D-Phe-OH; (2R)-2-[(tert-butoxy)carbonylamino]-3-phenylpropanoic acid; N-(t-butyloxycarbonyl)-D-Phenylalanine; Boc-phenylalanine; BOC-D-PHE; Boc-L-Phenylalanine; (2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoic acid; N-Boc-D-phenylalanine; (S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropanoic acid; N-(tert-Butoxycarbonyl)-L-phenylalanine; boc-L-Phe; MFCD00063149; N-t-Butyloxycarbonyl-L-phenylalanine; N-α-t-BOC-L-phenylalanine; N-(t-Butyloxycarbonyl)-R-phenylalanine; (R)-N-(tert-butoxycarbonyl)phenylalanine; N-tert-Butyloxycarbonyl-L-phenylalanine; Boc-D-phenylalanine; N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-phenylalanine; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid; N-(tert-butoxycarbonyl)-D-phenylalanine; N-(tert-Butoxycarbonyl)-L-phenylala |
| Molecular Formula | C14H19NO4 |
| Molecular Weight | 265.30 |
| Purity | ≥99.0 (sum of enantiomers, TLC) |
| Density | 1.2±0.1 g/cm3 |
| Boiling Point | 426.6±38.0 °C at 760 mmHg |
| Melting Point | 85-88ºC |
| Appearance | White to off-white crystalline powder |
| Storage Condition | Sealed in a cool, dry environment of 2-8ºC |
| Application | Boc-D-Phe-OH is a phenylalanine derivative [1]. |
| HTC | 2924299090 |
| PubChem ID | 57647459 |
| MDL Number | MFCD00063149 |
| SMILES | CC(C)(C)OC(=O)N[C@H](Cc1ccccc1)C(O)=O |
| InChI | 1S/C14H19NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m1/s1 |
| InChI Key | ZYJPUMXJBDHSIF-LLVKDONJSA-N |
| Beilstein/REAXYS | 4695945 |
| NACRES Code | NA.22 |
| eCl@ss | 32160406 |
| UNSPSC | 12352209 |
| Hazard Symbols | Transport |
| Safety Description | S24/25 |
| MSDS | msds/8506_2_18942_49_9.pdf |
| Bioactivity | Boc-D-Phe-OH is a phenylalanine 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):1793-884. Chemical & Physical Properties Density 1.2±0.1 g/cm3 Boiling Point 426.6±38.0 °C at 760 mmHg Melting Point 85-88ºC Molecular Formula C14H19NO4 Molecular Weight 265.305 Flash Point 211.8±26.8 °C Exact Mass 265.131409 PSA 75.63000 LogP 2.96 Vapour Pressure 0.0±1.1 mmHg at 25°C Index of Refraction 1.528 InChIKey ZYJPUMXJBDHSIF-LLVKDONJSA-N SMILES CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)O Storage condition 2~8°C |
| Use of | Boc-D-Phe-OH is a phenylalanine derivative[1]. Properties Name (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid Synonym More Synonyms Boc-D-Phe-OH Biological Activity Description Boc-D-Phe-OH is a phenylalanine 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):1793-884. Chemical & Physical Properties Molecular Formula C14H19NO4 Exact Mass 265.131409 PSA 75.63000 Index of Refraction 1.528 InChIKey ZYJPUMXJBDHSIF-LLVKDONJSA-N |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: No dangerous goods IMDG Code: No dangerous goods International Air Transport Dangerous Regulations: No dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available |
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