O-TERT-BUTYL-L-SERINE TERT-BUTYL ESTER HYDROCHLORIDE
O-tert-Butyl-L-serine tert-butyl ester hydrochloride
CAS: 51537-21-4
Molecular Formula: C11H24ClNO3
O-TERT-BUTYL-L-SERINE TERT-BUTYL ESTER HYDROCHLORIDE - Names and Identifiers
O-TERT-BUTYL-L-SERINE TERT-BUTYL ESTER HYDROCHLORIDE - Physico-chemical Properties
| Molecular Formula | C11H24ClNO3 |
| Molar Mass | 253.77 |
| Melting Point | 170-177℃ |
| Appearance | Crystalline Solid |
| Color | White |
| BRN | 4886392 |
| Storage Condition | Inert atmosphere,2-8°C |
O-TERT-BUTYL-L-SERINE TERT-BUTYL ESTER HYDROCHLORIDE - Risk and Safety
| WGK Germany | 3 |
O-TERT-BUTYL-L-SERINE TERT-BUTYL ESTER HYDROCHLORIDE - Introduction
O-tert-Butyl-L-serine tert-butyl ester hydrochloride is an organic compound with the chemical formula C13H27ClN2O3. It is a solid and can be dissolved in water.
The compound is mainly used as an intermediate in organic synthesis and is commonly used in the synthesis of natural products with physiological activity. It has a wide range of applications in the field of medicine, such as the synthesis of serine-related drugs, anti-tumor drugs and other biologically active compounds.
The method for preparing the compound is generally obtained by reacting tert-butyl L-serine with hydrochloric acid. The specific preparation step may be to dissolve L-serine tert-butyl ester in a reaction solvent, then add a certain amount of hydrochloric acid, react for a period of time, and obtain the product by crystallization, filtration and other steps.
Regarding the safety information of this compound, it should be noted that it is an organic compound with certain toxicity. In the use and operation should follow the laboratory safety procedures. Avoid contact with skin and inhalation of dust or gas. Should be sealed in storage, away from fire and flammable materials, avoid contact with oxidants and strong acid. If exposed or inhaled, seek medical attention immediately.
The compound is mainly used as an intermediate in organic synthesis and is commonly used in the synthesis of natural products with physiological activity. It has a wide range of applications in the field of medicine, such as the synthesis of serine-related drugs, anti-tumor drugs and other biologically active compounds.
The method for preparing the compound is generally obtained by reacting tert-butyl L-serine with hydrochloric acid. The specific preparation step may be to dissolve L-serine tert-butyl ester in a reaction solvent, then add a certain amount of hydrochloric acid, react for a period of time, and obtain the product by crystallization, filtration and other steps.
Regarding the safety information of this compound, it should be noted that it is an organic compound with certain toxicity. In the use and operation should follow the laboratory safety procedures. Avoid contact with skin and inhalation of dust or gas. Should be sealed in storage, away from fire and flammable materials, avoid contact with oxidants and strong acid. If exposed or inhaled, seek medical attention immediately.
Last Update：2024-04-09 19:05:53
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View History
O-TERT-BUTYL-L-SERINE TERT-BUTYL ESTER HYDROCHLORIDE
2-甲氧乙氧基甲基氯
HYDROCHLORIC ACID - STANDARD VOLUMETRIC SOLUTION (0.5 M) IN NON-DENATURED ETHANOL (99.5 %)
6-Acetoxyhexanoic acid ethyl ester
3,4-二甲氧基苯乙胺
2-甲氧乙氧基甲基氯
HYDROCHLORIC ACID - STANDARD VOLUMETRIC SOLUTION (0.5 M) IN NON-DENATURED ETHANOL (99.5 %)
6-Acetoxyhexanoic acid ethyl ester
3,4-二甲氧基苯乙胺