(S)-2-(tert-butoxycarbonylamino)-3-phenylpropymethanesulfonate
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropymethanesulfonate
CAS: 109687-66-3
Molecular Formula: C15H23NO5S
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropymethanesulfonate - Names and Identifiers
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropymethanesulfonate - Physico-chemical Properties
| Molecular Formula | C15H23NO5S |
| Molar Mass | 329.41 |
| Density | 1.185±0.06 g/cm3(Predicted) |
| Melting Point | 116-117 °C (decomp) |
| Boling Point | 511.8±50.0 °C(Predicted) |
| pKa | 11.62±0.46(Predicted) |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD22420226 |
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropymethanesulfonate - Introduction
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropyl methanesulfonate is an organic compound whose chemical structure can be represented by: CH3CH2C(CH3)C6H4CH2NHCOOC(CH3)CH2SO3H.
Nature:
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonate is a solid substance, sometimes also in the form of white to yellowish-white crystals. It has high thermal stability and water solubility. The chemical properties of this compound make it play an important role in many organic synthesis reactions and drug synthesis.
Use:
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonate is widely used in the pharmaceutical industry as a synthetic intermediate. It is often used in the synthesis of amino acids, peptides, drugs and bioactive molecules. In addition, it can also be used as a ligand for a chiral support catalyst.
Preparation Method:
The preparation method of (S)-2-(tert-butoxycarbonylamino)-3-phenylpropyl methanesulfonate can be achieved by the following steps:
1. (S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonic acid is prepared by an appropriate method.
2. (S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonic acid reacts with a certain amount of sodium carbonate to generate the corresponding sulfonate.
Safety Information:
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonate is not particularly hazardous under normal conditions, but as a chemical substance, appropriate safety measures need to be taken during use and handling. It is recommended to wear protective gloves, glasses and laboratory coats during operation. In case of accidental contact with skin or eyes, rinse immediately with plenty of water and seek medical advice. The compound must be stored and handled properly to avoid contact with substances such as oxidizing agents.
Nature:
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonate is a solid substance, sometimes also in the form of white to yellowish-white crystals. It has high thermal stability and water solubility. The chemical properties of this compound make it play an important role in many organic synthesis reactions and drug synthesis.
Use:
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonate is widely used in the pharmaceutical industry as a synthetic intermediate. It is often used in the synthesis of amino acids, peptides, drugs and bioactive molecules. In addition, it can also be used as a ligand for a chiral support catalyst.
Preparation Method:
The preparation method of (S)-2-(tert-butoxycarbonylamino)-3-phenylpropyl methanesulfonate can be achieved by the following steps:
1. (S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonic acid is prepared by an appropriate method.
2. (S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonic acid reacts with a certain amount of sodium carbonate to generate the corresponding sulfonate.
Safety Information:
(S)-2-(tert-butoxycarbonylamino)-3-phenylpropylmethanesulfonate is not particularly hazardous under normal conditions, but as a chemical substance, appropriate safety measures need to be taken during use and handling. It is recommended to wear protective gloves, glasses and laboratory coats during operation. In case of accidental contact with skin or eyes, rinse immediately with plenty of water and seek medical advice. The compound must be stored and handled properly to avoid contact with substances such as oxidizing agents.
Last Update：2024-04-09 20:52:54
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