BOC-4-甲氧基-L-苯丙氨酸
Boc-O-methyl-L-tyrosine
CAS: 53267-93-9
Molecular Formula: C15H21NO5
BOC-4-甲氧基-L-苯丙氨酸 - Names and Identifiers
| Name | Boc-O-methyl-L-tyrosine |
| Synonyms | BOC-L-TYR(ME) Boc-Tyr(Me)-OH BOC-L-TYR(ME)-OH BOC-PHE(4-OME)-OH BOC-L-4-METHOXYPHE BOC-P-METHOXY-PHE-OH BOC-4-METHOXY-PHE-OH Boc-O-methyl-L-tyrosine BOC-O-METHYL-L-TYROSINE BOC-4-METHOXYPHENYLALANINE L-4'-Methoxy-N-Boc-tyrosine Boc-L-4-Methoxyphenylalanine Boc-4-Methoxy-L-phenylalanine N-(tert-butoxycarbonyl)-O-methyl-L-tyrosine N-(tert-butoxycarbonyl)-4-methoxyphenylalanine 1-(tert-butoxycarbonyl)-2-(furan-2-ylmethyl)-L-proline (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(4-methoxyphenyl)propanoic acid |
| CAS | 53267-93-9 |
| InChI | InChI=1/C15H21NO5/c1-15(2,3)21-14(19)16-12(13(17)18)9-10-5-7-11(20-4)8-6-10/h5-8,12H,9H2,1-4H3,(H,16,19)(H,17,18)/t12-/m0/s1 |
BOC-4-甲氧基-L-苯丙氨酸 - Physico-chemical Properties
| Molecular Formula | C15H21NO5 |
| Molar Mass | 295.33 |
| Density | 1.168±0.06 g/cm3(Predicted) |
| Boling Point | 462.0±40.0 °C(Predicted) |
| Flash Point | 233.2°C |
| Vapor Presure | 2.47E-09mmHg at 25°C |
| Appearance | Solid |
| pKa | 3.00±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.522 |
| MDL | MFCD00065603 |
BOC-4-甲氧基-L-苯丙氨酸 - Risk and Safety
| WGK Germany | 3 |
| HS Code | 2924 29 70 |
| Hazard Class | IRRITANT |
BOC-4-甲氧基-L-苯丙氨酸 - Introduction
Boc-O-methyl-L-tyrosine(Boc-O-methyl-L-tyrosine) is an organic compound whose chemical formula is C15H21NO5. It is a derivative of L-tyrosine with a protecting group Boc(tert-butyloxycarbonyl) attached to the amino group. The Boc group can protect the amino group to prevent accidental reactions with other reactants.
Boc-O-methyl-L-tyrosine are useful in pharmaceutical research and chemical synthesis. It is often used as a protecting group in polypeptide synthesis to control the positional selectivity of the reaction. In addition, it can also be used as a synthetic intermediate for some potential drugs in the pharmaceutical field.
The preparation of Boc-O-methyl-L-tyrosine is usually accomplished by adding a Boc protecting group to the amino group of L-tyrosine. This step can be carried out by chemical synthesis, and the specific reaction conditions and catalysts will vary.
When using Boc-O-methyl-L-tyrosine, pay attention to its safety. It may cause irritation to the eyes, skin and respiratory tract and direct contact should be avoided. Appropriate protective measures should be taken during operation, such as wearing gloves, goggles and masks. In addition, it should be stored in a dry, well-ventilated place, away from fire and oxidizing agents. In case of accidental contact or inhalation, seek medical attention immediately. When using this compound, it is necessary to follow the safe operating procedures of the chemical laboratory.
Boc-O-methyl-L-tyrosine are useful in pharmaceutical research and chemical synthesis. It is often used as a protecting group in polypeptide synthesis to control the positional selectivity of the reaction. In addition, it can also be used as a synthetic intermediate for some potential drugs in the pharmaceutical field.
The preparation of Boc-O-methyl-L-tyrosine is usually accomplished by adding a Boc protecting group to the amino group of L-tyrosine. This step can be carried out by chemical synthesis, and the specific reaction conditions and catalysts will vary.
When using Boc-O-methyl-L-tyrosine, pay attention to its safety. It may cause irritation to the eyes, skin and respiratory tract and direct contact should be avoided. Appropriate protective measures should be taken during operation, such as wearing gloves, goggles and masks. In addition, it should be stored in a dry, well-ventilated place, away from fire and oxidizing agents. In case of accidental contact or inhalation, seek medical attention immediately. When using this compound, it is necessary to follow the safe operating procedures of the chemical laboratory.
Last Update：2024-04-09 20:52:54
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View History
BOC-4-甲氧基-L-苯丙氨酸
2-氰基-6-氟苯基硼酸
苄基-2-乙酰氨基-3,6-二-O-苄基-2-脱氧-α-D-吡喃葡萄糖苷
TETRAMETHYLAMMONIUM CHLORIDE, FOR MOLECU LAR BIOLOGY
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5-氨基-2-甲氧基苯酚
2-氟-20-(甲硫基)吡啶
2-氯-5-氟-4-甲基嘧啶
2-甲氧基-3-甲基吡啶
(VOI)4-氯吡啶-2,6-二羧酸
2-氰基-6-氟苯基硼酸
苄基-2-乙酰氨基-3,6-二-O-苄基-2-脱氧-α-D-吡喃葡萄糖苷
TETRAMETHYLAMMONIUM CHLORIDE, FOR MOLECU LAR BIOLOGY
(2S,5R,6R)-6-[[(2R)-羧基-3-噻吩基乙酰]氨基]-3,3-二甲基-7-氧代-4-硫杂-1-氮杂二环[3.2.0]庚烷-2-羧酸二钠盐
5-氨基-2-甲氧基苯酚
2-氟-20-(甲硫基)吡啶
2-氯-5-氟-4-甲基嘧啶
2-甲氧基-3-甲基吡啶
(VOI)4-氯吡啶-2,6-二羧酸