BOC-PHE(4-OET)-OH
N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine
CAS: 76757-91-0
Molecular Formula: C16H23NO5
BOC-PHE(4-OET)-OH - Names and Identifiers
| Name | N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine |
| Synonyms | BOC-TYR-OET Boc-Tyr-OEt BOC-TYR(ET)-OH Boc-Tyr(Et)-OH BOC-PHE(4-OET)-OH BOC-TYROSINE(ET)-OH N-ALPHA-T-BOC-O-ETHYL-L-TYROSINE N-(TERT-BUTOXYCARBONYL)-O-ETHYLTYROSINE N-(tert-Butoxycarbonyl)-O-ethyl-L-tyrosine N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine N-ALPHA-T-BUTOXYCARBONYL-O-ETHYL-L-TYROSINE L-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-O-ethyl- (2S)-3-(4-ethoxyphenyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoic acid |
| CAS | 76757-91-0 |
| InChI | InChI=1/C16H23NO5/c1-5-21-12-8-6-11(7-9-12)10-13(14(18)19)17-15(20)22-16(2,3)4/h6-9,13H,5,10H2,1-4H3,(H,17,20)(H,18,19)/t13-/m0/s1 |
BOC-PHE(4-OET)-OH - Physico-chemical Properties
| Molecular Formula | C16H23NO5 |
| Molar Mass | 309.36 |
| Density | 1.149g/cm3 |
| Boling Point | 472.7°C at 760 mmHg |
| Flash Point | 239.7°C |
| Vapor Presure | 9.7E-10mmHg at 25°C |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.519 |
BOC-PHE(4-OET)-OH - Risk and Safety
| WGK Germany | 3 |
| Hazard Class | IRRITANT |
BOC-PHE(4-OET)-OH - Introduction
N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine, chemical formula C15H21NO6, is an organic compound. Its properties are as follows:
1. Appearance: N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine is a white crystalline powder.
2. Solubility: It can be dissolved in common organic solvents, such as methanol, ethanol and dichloromethane.
3. Storage stability: As a solid, it should be stored in a dry, cool place, away from fire and oxygen. It can be stored stably under suitable conditions.
N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine are mainly used in biomedical research and drug synthesis.
1. Biomedical research: The compound has important application value in drug development and protein engineering. It can be used in the synthesis of peptide drugs or as a protein stabilizer.
2. Drug synthesis: N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine can be used as an intermediate for the synthesis of other organic compounds or drugs.
The preparation of N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine is usually carried out by organic synthetic chemical reactions. The specific preparation method may include the following steps:
1. acid chloride formation: under suitable conditions, tyrosine and tert-butoxycarbonyl chloride react to generate acid chloride intermediate.
2. Acid chloride reaction: The acid chloride intermediate is reacted with appropriate ethanol to form N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine.
Safety Information:
1. N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine is a chemical and should be used in appropriate laboratory facilities and safe practices.
2. Appropriate personal protective equipment, such as lab gloves, goggles and lab clothes, should be provided during use.
3. Avoid direct contact with skin and eyes. If there is contact, rinse immediately with plenty of water.
4. avoid inhalation of dust or gas, to ensure that the operating place is well ventilated.
5. for the use and handling of this chemical, should comply with the relevant laws and regulations and safety procedures.
1. Appearance: N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine is a white crystalline powder.
2. Solubility: It can be dissolved in common organic solvents, such as methanol, ethanol and dichloromethane.
3. Storage stability: As a solid, it should be stored in a dry, cool place, away from fire and oxygen. It can be stored stably under suitable conditions.
N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine are mainly used in biomedical research and drug synthesis.
1. Biomedical research: The compound has important application value in drug development and protein engineering. It can be used in the synthesis of peptide drugs or as a protein stabilizer.
2. Drug synthesis: N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine can be used as an intermediate for the synthesis of other organic compounds or drugs.
The preparation of N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine is usually carried out by organic synthetic chemical reactions. The specific preparation method may include the following steps:
1. acid chloride formation: under suitable conditions, tyrosine and tert-butoxycarbonyl chloride react to generate acid chloride intermediate.
2. Acid chloride reaction: The acid chloride intermediate is reacted with appropriate ethanol to form N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine.
Safety Information:
1. N-(tert-butoxycarbonyl)-O-ethyl-L-tyrosine is a chemical and should be used in appropriate laboratory facilities and safe practices.
2. Appropriate personal protective equipment, such as lab gloves, goggles and lab clothes, should be provided during use.
3. Avoid direct contact with skin and eyes. If there is contact, rinse immediately with plenty of water.
4. avoid inhalation of dust or gas, to ensure that the operating place is well ventilated.
5. for the use and handling of this chemical, should comply with the relevant laws and regulations and safety procedures.
Last Update：2024-04-09 21:22:08
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CAS: 76757-91-0
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CAS: 76757-91-0
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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