Carbamic acid, N-[1-(4-boronophenyl)cyclopropyl]-, C-(1,1-dimethylethyl) ester
(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid
CAS: 1217500-58-7
Molecular Formula: C14H20BNO4
Carbamic acid, N-[1-(4-boronophenyl)cyclopropyl]-, C-(1,1-dimethylethyl) ester - Names and Identifiers
Carbamic acid, N-[1-(4-boronophenyl)cyclopropyl]-, C-(1,1-dimethylethyl) ester - Physico-chemical Properties
| Molecular Formula | C14H20BNO4 |
| Molar Mass | 277.12 |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD12546458 |
Carbamic acid, N-[1-(4-boronophenyl)cyclopropyl]-, C-(1,1-dimethylethyl) ester - Introduction
(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl) boronic acid, also known as (4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid, is an organic compound. Its nature, use, formulation and safety information are described below.
1. Nature
(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid is a solid compound with a chemical formula of C20H31BN2O5. It is white or white crystal, soluble in some organic solvents such as acetone, dichloromethane and so on. It is a boronic acid derivative containing both ester and amine groups.
2. use
This compound is an important intermediate in organic synthesis, which is used to synthesize a variety of organic compounds, especially in drug research and development. It is often used as a coupling reagent in organic synthesis, especially in the chemical reactions of phenylboronic acid, such as Suzuki coupling reaction and Stille coupling reaction.
3. Preparation method
(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid is generally synthesized by organic synthesis methods. The specific method is to react pyridyl borate with tert-butyl 1-aminocyclopropane -1-carboxylate to generate the target product.
4. Safety Information
Regarding the safety of this compound, general laboratory safety operations should be followed. It may be irritating to the skin, eyes and respiratory tract and should be avoided. Appropriate protective equipment such as gloves, goggles and lab coats are required for use. In addition, the compound should be handled in a well-ventilated area to avoid inhalation of its vapors. If exposed or inhaled, seek medical help immediately.
Please note that when using and handling chemical substances, relevant safety information and operating instructions should always be understood and followed.
1. Nature
(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid is a solid compound with a chemical formula of C20H31BN2O5. It is white or white crystal, soluble in some organic solvents such as acetone, dichloromethane and so on. It is a boronic acid derivative containing both ester and amine groups.
2. use
This compound is an important intermediate in organic synthesis, which is used to synthesize a variety of organic compounds, especially in drug research and development. It is often used as a coupling reagent in organic synthesis, especially in the chemical reactions of phenylboronic acid, such as Suzuki coupling reaction and Stille coupling reaction.
3. Preparation method
(4-(1-((tert-Butoxycarbonyl)amino)-cyclopropyl)phenyl)boronic acid is generally synthesized by organic synthesis methods. The specific method is to react pyridyl borate with tert-butyl 1-aminocyclopropane -1-carboxylate to generate the target product.
4. Safety Information
Regarding the safety of this compound, general laboratory safety operations should be followed. It may be irritating to the skin, eyes and respiratory tract and should be avoided. Appropriate protective equipment such as gloves, goggles and lab coats are required for use. In addition, the compound should be handled in a well-ventilated area to avoid inhalation of its vapors. If exposed or inhaled, seek medical help immediately.
Please note that when using and handling chemical substances, relevant safety information and operating instructions should always be understood and followed.
Last Update：2024-04-09 21:54:55
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