2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-(4-phenylmethoxyphenyl)propanoic acid
Boc-D-Tyr(Bzl)-OH
CAS: 63769-58-4
Molecular Formula: C21H25NO5
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-(4-phenylmethoxyphenyl)propanoic acid - Names and Identifiers
| Name | Boc-D-Tyr(Bzl)-OH |
| Synonyms | BOC-D-TYR(BZL)-OH Boc-D-Tyr(Bzl)-OH BOC-D-TYROSINE(BZL)-OH N-ALPHA-T-BOC-O-BENZYL-D-TYROSINE O-benzyl-N-(tert-butoxycarbonyl)-D-tyrosine N-ALPHA-T-BUTOXYCARBONYL-O-BENZYL-D-TYROSINE N-ALPHA-TERT-BUTYLOXYCARBONYL-O-BENZYL-D-TYROSINE BOC-(R)-2-AMINO-3-(4'-BENZYLOXYPHENYL)PROPANOIC ACID (2R)-3-[4-(benzyloxy)phenyl]-2-{[(tert-butoxy)carbonyl]amino}propanoic acid 2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-(4-phenylmethoxyphenyl)propanoic acid |
| CAS | 63769-58-4 |
| InChI | InChI=1/C21H25NO5/c1-21(2,3)27-20(25)22-18(19(23)24)13-15-9-11-17(12-10-15)26-14-16-7-5-4-6-8-16/h4-12,18H,13-14H2,1-3H3,(H,22,25)(H,23,24)/t18-/m1/s1 |
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-(4-phenylmethoxyphenyl)propanoic acid - Physico-chemical Properties
| Molecular Formula | C21H25NO5 |
| Molar Mass | 371.43 |
| Density | 1.185±0.06 g/cm3(Predicted) |
| Boling Point | 552.4±50.0 °C(Predicted) |
| Flash Point | 287.9°C |
| Water Solubility | Slightly soluble in water. |
| Vapor Presure | 4.87E-13mmHg at 25°C |
| Appearance | Solid |
| pKa | 2.99±0.10(Predicted) |
| Storage Condition | Store below +30°C. |
| Refractive Index | 1.562 |
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-(4-phenylmethoxyphenyl)propanoic acid - Introduction
Boc-D-Tyr(Bzl)-OH(Boc-D-Tyr(Bzl)-OH) is an organic compound. Its chemical properties are similar to other Boc protected amino acids.
Boc-D-Tyr(Bzl)-OH is a D-tyrosine derivative having a protecting group (Boc). It can be used as a starting material or intermediate for peptide synthesis. Boc protecting groups can protect the amide nitrogen or other functional groups during the synthesis to prevent non-specific reactions from occurring. In addition, Boc-D-Tyr(Bzl)-OH can also be used in pharmaceutical research and synthesis of bioactive peptides.
A common method of preparing Boc-D-Tyr(Bzl)-OH is by reacting an N-alpha protected tyrosine with benzyl alcohol. First, the amino group of tyrosine is protected and then reacted with benzyl alcohol under appropriate conditions to form the desired product. Finally, the protecting group of the amino group is removed to give the Boc-D-Tyr(Bzl)-OH.
Regarding safety information, Boc-D-Tyr(Bzl)-OH is a chemical that needs to be operated in a laboratory and comply with relevant laboratory safety operating regulations. It may be irritating to the skin, eyes and respiratory system, so personal protective equipment such as lab gloves and protective glasses should be worn. When handling and storing compounds, care should be taken to avoid contact with ignition sources or other flammable materials. If inhaled or entered into the eyes or mouth, rinse immediately with plenty of water and seek medical assistance as needed.
Boc-D-Tyr(Bzl)-OH is a D-tyrosine derivative having a protecting group (Boc). It can be used as a starting material or intermediate for peptide synthesis. Boc protecting groups can protect the amide nitrogen or other functional groups during the synthesis to prevent non-specific reactions from occurring. In addition, Boc-D-Tyr(Bzl)-OH can also be used in pharmaceutical research and synthesis of bioactive peptides.
A common method of preparing Boc-D-Tyr(Bzl)-OH is by reacting an N-alpha protected tyrosine with benzyl alcohol. First, the amino group of tyrosine is protected and then reacted with benzyl alcohol under appropriate conditions to form the desired product. Finally, the protecting group of the amino group is removed to give the Boc-D-Tyr(Bzl)-OH.
Regarding safety information, Boc-D-Tyr(Bzl)-OH is a chemical that needs to be operated in a laboratory and comply with relevant laboratory safety operating regulations. It may be irritating to the skin, eyes and respiratory system, so personal protective equipment such as lab gloves and protective glasses should be worn. When handling and storing compounds, care should be taken to avoid contact with ignition sources or other flammable materials. If inhaled or entered into the eyes or mouth, rinse immediately with plenty of water and seek medical assistance as needed.
Last Update：2024-04-09 21:01:54
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View History
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-(4-phenylmethoxyphenyl)propanoic acid
2,4-双(1-甲基-1-苯乙基)苯酚
4-SEC-BUTYL-2-BROMOPHENOL
(2-Amino-tert-butyl)carbamic acid tert-butyl ester monohydrochloride
Caustic soda flake
2-HYDROXY-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE
(4-chlorophenyl)(2-hydroxyphenyl)methanone
1,2-二氢-6-羟基-2-氧代-3-氰基吡啶
7-氧代庚基乙酸酯
dipotassium tetraoxomolybdate
2,4-双(1-甲基-1-苯乙基)苯酚
4-SEC-BUTYL-2-BROMOPHENOL
(2-Amino-tert-butyl)carbamic acid tert-butyl ester monohydrochloride
Caustic soda flake
2-HYDROXY-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE
(4-chlorophenyl)(2-hydroxyphenyl)methanone
1,2-二氢-6-羟基-2-氧代-3-氰基吡啶
7-氧代庚基乙酸酯
dipotassium tetraoxomolybdate