氧羰基-D-酪氨酸-甲氧基酯
boc-D-tyrosine methyl ester
CAS: 76757-90-9
Molecular Formula: C15H21NO5
氧羰基-D-酪氨酸-甲氧基酯 - Names and Identifiers
| Name | boc-D-tyrosine methyl ester |
| Synonyms | Boc-D-Tyr-OMe BOC-D-TYR-OME boc-D-tyrosine methyl ester N-BOC-D-tyrosine methyl ester N-T-boc-D-tyrosine methyl ester methyl N-(tert-butoxycarbonyl)-D-tyrosinate Methyl (R)-2-[(tert-Butoxycarbonyl)amino]-3-(4-hydroxyphenyl)propionate methyl (2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(4-hydroxyphenyl)propanoate methyl (2R)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate |
| CAS | 76757-90-9 |
| EINECS | 201-525-2 |
| InChI | InChI=1/C15H21NO5/c1-15(2,3)21-14(19)16-12(13(18)20-4)9-10-5-7-11(17)8-6-10/h5-8,12,17H,9H2,1-4H3,(H,16,19)/t12-/m1/s1 |
氧羰基-D-酪氨酸-甲氧基酯 - Physico-chemical Properties
| Molecular Formula | C15H21NO5 |
| Molar Mass | 295.33 |
| Density | 1.169±0.06 g/cm3(Predicted) |
| Boling Point | 452.7±40.0 °C(Predicted) |
| Flash Point | 227.6°C |
| Vapor Presure | 8.19E-09mmHg at 25°C |
| Appearance | Powder |
| Color | White |
| pKa | 9.75±0.15(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | 1.523 |
氧羰基-D-酪氨酸-甲氧基酯 - Risk and Safety
| WGK Germany | 3 |
氧羰基-D-酪氨酸-甲氧基酯 - Introduction
boc-D-tyrosine methyl ester is an organic compound with the chemical formula C17H23NO5. It is the N-protecting methyl ester compound of D-tyrosine, wherein Boc represents N-tert-butoxycarbonyl (tert-butoxycarbonyl). boc-D-tyrosine ester is a common amino acid protecting group, which can protect nucleophile from reacting with D-tyrosine in synthesis.
The main use of boc-D-tyrosine methyl ester is as a starting material or intermediate in polypeptide synthesis, and is used to synthesize polypeptides containing D-tyrosine. This can be achieved by adding a N-tert-butoxycarbonyl methyl group to D-tyrosine.
The method of preparing boc-D-tyrosine methyl ester can use a variety of different reaction conditions. A common synthetic method is to react D-tyrosine with methanol and sulfuric acid to produce D-tyrosine methyl ester, which is then reacted with N-tert-butoxycarbonyl isocyanate to produce boc-D-tyrosine ester.
Regarding safety information, boc-D-tyrosine methyl ester is generally relatively safe under appropriate operating conditions. However, it is an organic compound that is potentially irritating and toxic. Use should follow appropriate laboratory safety practices, such as wearing protective gloves, glasses, and laboratory coats, and operate in a well-ventilated environment. Use chemical protective equipment and engineering controls as necessary to protect personal safety.
The main use of boc-D-tyrosine methyl ester is as a starting material or intermediate in polypeptide synthesis, and is used to synthesize polypeptides containing D-tyrosine. This can be achieved by adding a N-tert-butoxycarbonyl methyl group to D-tyrosine.
The method of preparing boc-D-tyrosine methyl ester can use a variety of different reaction conditions. A common synthetic method is to react D-tyrosine with methanol and sulfuric acid to produce D-tyrosine methyl ester, which is then reacted with N-tert-butoxycarbonyl isocyanate to produce boc-D-tyrosine ester.
Regarding safety information, boc-D-tyrosine methyl ester is generally relatively safe under appropriate operating conditions. However, it is an organic compound that is potentially irritating and toxic. Use should follow appropriate laboratory safety practices, such as wearing protective gloves, glasses, and laboratory coats, and operate in a well-ventilated environment. Use chemical protective equipment and engineering controls as necessary to protect personal safety.
Last Update：2024-04-10 22:29:15
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View History
氧羰基-D-酪氨酸-甲氧基酯
5-溴-7H-苯并[C]咔唑
(2-me(2-methoxyethyl)hydrazinethoxyethyl)hydrazine
7-氨基-3-氰基吡唑并[1,5-A]嘧啶-6-羧酸乙酯
2-氨基-3-乙酰基苯酚
4-((((9H-芴-9-基)甲氧基)羰基)氨基)四氢-2H-噻喃-4-羧酸
5-溴-7H-苯并[C]咔唑
(2-me(2-methoxyethyl)hydrazinethoxyethyl)hydrazine
7-氨基-3-氰基吡唑并[1,5-A]嘧啶-6-羧酸乙酯
2-氨基-3-乙酰基苯酚
4-((((9H-芴-9-基)甲氧基)羰基)氨基)四氢-2H-噻喃-4-羧酸