(R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxyphenyl)propanoic acid
(2R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxy-phenyl)propanoic acid
CAS: 478183-57-2
Molecular Formula: C14H18ClNO5
(R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxyphenyl)propanoic acid - Names and Identifiers
| Name | (2R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxy-phenyl)propanoic acid |
| Synonyms | Boc-D-Tyr(3-Cl)-OH Boc-D-3-Chlorotyrosine 3-Chloro-N-Boc-D-tyrosine N-Boc-3-Chloro-D-Tyrosine Boc-3-chloro-D-Tyr-OH·DCHA Boc-3-chloro-D-tyrosine DCHA (R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxyphenyl)propanoic acid (2R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxy-phenyl)propanoic acid (2R)-3-(3-chloro-4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoicaci (2R)-3-(3-chloro-4-hydroxyphenyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoic acid |
| CAS | 478183-57-2 |
| InChI | InChI=1/C14H18ClNO5/c1-14(2,3)21-13(20)16-10(12(18)19)7-8-4-5-11(17)9(15)6-8/h4-6,10,17H,7H2,1-3H3,(H,16,20)(H,18,19)/t10-/m1/s1 |
(R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxyphenyl)propanoic acid - Physico-chemical Properties
| Molecular Formula | C14H18ClNO5 |
| Molar Mass | 315.75 |
| Density | 1.321g/cm3 |
| Boling Point | 490.6°C at 760 mmHg |
| Flash Point | 250.5°C |
| Vapor Presure | 1.94E-10mmHg at 25°C |
| Storage Condition | Store at?0-5°C |
| Refractive Index | 1.559 |
(R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxyphenyl)propanoic acid - Introduction
(2R)-2-(tert-butoxycarbonylamino)-3-(-) propanoic acid is a compound whose chemical name is (2R)-2-(tert-butoxycarbonylamino)-3-(-) propanoic acid. Its molecular formula is C15H19ClNO5 and its molecular weight is 331.77.
It is a white crystalline solid with a distinctive odor. It is soluble in some organic solvents at room temperature, such as methanol and dimethyl sulfoxide.
(2R)-2-(tert-butoxycarbonylamino)-3-(2R) propanoic acid is an important amino acid derivative commonly used in biomedical research. It can be used as an intermediate in the synthesis of drugs, such as antibiotics, rumen hormones and peptide antibodies. In addition, it is also commonly used to study the metabolic pathways of cancer drugs and tyrosine.
(2R)-2-(tert-butoxycarbonylamino)-3-(2R) propanoic acid is mainly prepared by chemical synthesis. A common method is to react p-hydroxybenzoic acid with Boc-protected D-tyrosine and carry out condensation reaction under appropriate conditions to obtain the target product.
Pay attention to safety precautions when using and handling (2R)-2-(tert-butoxycarbonylamino)-3-(2R) propanoic acid. It may cause irritation and damage to the skin, eyes and respiratory system. Appropriate personal protective equipment, such as gloves and goggles, should be worn during operation. Avoid inhaling its dust or vapors, and avoid contact with skin and eyes. In case of accidental contact, rinse immediately with plenty of water and seek medical help. In addition, avoid contact with oxidants and strong acids during storage, and regularly check the integrity of the container.
It is a white crystalline solid with a distinctive odor. It is soluble in some organic solvents at room temperature, such as methanol and dimethyl sulfoxide.
(2R)-2-(tert-butoxycarbonylamino)-3-(2R) propanoic acid is an important amino acid derivative commonly used in biomedical research. It can be used as an intermediate in the synthesis of drugs, such as antibiotics, rumen hormones and peptide antibodies. In addition, it is also commonly used to study the metabolic pathways of cancer drugs and tyrosine.
(2R)-2-(tert-butoxycarbonylamino)-3-(2R) propanoic acid is mainly prepared by chemical synthesis. A common method is to react p-hydroxybenzoic acid with Boc-protected D-tyrosine and carry out condensation reaction under appropriate conditions to obtain the target product.
Pay attention to safety precautions when using and handling (2R)-2-(tert-butoxycarbonylamino)-3-(2R) propanoic acid. It may cause irritation and damage to the skin, eyes and respiratory system. Appropriate personal protective equipment, such as gloves and goggles, should be worn during operation. Avoid inhaling its dust or vapors, and avoid contact with skin and eyes. In case of accidental contact, rinse immediately with plenty of water and seek medical help. In addition, avoid contact with oxidants and strong acids during storage, and regularly check the integrity of the container.
Last Update：2024-04-09 20:52:54
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