carbamic acid, [(4-bromophenyl)methyl]methyl-, 1,1-dimethylethyl ester
(4-Bromo-benzyl)-methyl-carbamic acid tert-butyl ester
CAS: 260809-26-5
Molecular Formula: C13H18BrNO2
carbamic acid, [(4-bromophenyl)methyl]methyl-, 1,1-dimethylethyl ester - Names and Identifiers
carbamic acid, [(4-bromophenyl)methyl]methyl-, 1,1-dimethylethyl ester - Physico-chemical Properties
| Molecular Formula | C13H18BrNO2 |
| Molar Mass | 300.19 |
| Density | 1.295±0.06 g/cm3(Predicted) |
| Boling Point | 354.5±21.0 °C(Predicted) |
| pKa | -1.48±0.70(Predicted) |
carbamic acid, [(4-bromophenyl)methyl]methyl-, 1,1-dimethylethyl ester - Introduction
(4-Bromo-benzyl)-methyl-carbamic acid tert-butyl ester is an organic compound commonly abbreviated as BBMTBE. The following is a description of its nature, use, preparation and safety information:
Nature:
(4-Bromo-benzyl)-methyl-carbamic acid tert-butyl ester is a solid compound, usually white or light yellow crystals. It has low solubility and is soluble in organic solvents such as ethanol and dichloromethane at room temperature. Its molecular formula is C12H16BrNO2.
Use:
(4-Bromo-benzyl)-methyl-carbamic acid tert-butyl ester is commonly used as an intermediate in chemical research and synthesis. It can be used in organic synthesis reactions, such as Catalyst modification, compound synthesis and construction, etc. In addition, it can also be applied to the pharmaceutical industry for drug synthesis.
Method:
(4-Bromo-benzyl)-The preparation of methyl-carbamic acid tert-butyl ester can be completed by chemical reaction. Specific preparation methods generally involve intermolecular or intramolecular reactions, such as alcohol amine reactions or electrophilic substitution reactions catalyzed by acids. The preparation method is cumbersome and requires attention to safe operation and process conditions.
Safety Information:
When operating (4-Bromo-benzyl)-methyl-carbamic acid tert-butyl ester, comply with general laboratory safety regulations. It is less toxic, but care is still needed to avoid direct contact with the skin, eyes and respiratory tract. Personal protective equipment such as lab gloves, goggles and face shields should be worn during use to ensure well-ventilated lab conditions. In case of inadvertent contact, immediately flush the affected area with plenty of water and seek medical help.
Nature:
(4-Bromo-benzyl)-methyl-carbamic acid tert-butyl ester is a solid compound, usually white or light yellow crystals. It has low solubility and is soluble in organic solvents such as ethanol and dichloromethane at room temperature. Its molecular formula is C12H16BrNO2.
Use:
(4-Bromo-benzyl)-methyl-carbamic acid tert-butyl ester is commonly used as an intermediate in chemical research and synthesis. It can be used in organic synthesis reactions, such as Catalyst modification, compound synthesis and construction, etc. In addition, it can also be applied to the pharmaceutical industry for drug synthesis.
Method:
(4-Bromo-benzyl)-The preparation of methyl-carbamic acid tert-butyl ester can be completed by chemical reaction. Specific preparation methods generally involve intermolecular or intramolecular reactions, such as alcohol amine reactions or electrophilic substitution reactions catalyzed by acids. The preparation method is cumbersome and requires attention to safe operation and process conditions.
Safety Information:
When operating (4-Bromo-benzyl)-methyl-carbamic acid tert-butyl ester, comply with general laboratory safety regulations. It is less toxic, but care is still needed to avoid direct contact with the skin, eyes and respiratory tract. Personal protective equipment such as lab gloves, goggles and face shields should be worn during use to ensure well-ventilated lab conditions. In case of inadvertent contact, immediately flush the affected area with plenty of water and seek medical help.
Last Update：2024-04-09 19:05:48
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