27489-63-0
benzyl (trans-4-hydroxycyclohexyl)carbamate
CAS: 27489-63-0
Molecular Formula: C14H19NO3
27489-63-0 - Names and Identifiers
| Name | benzyl (trans-4-hydroxycyclohexyl)carbamate |
| Synonyms | LogP TRANS-4-CBZ-AMINOPHENOL trans-N-Cbz-4-aminocyclohexanol TRANS-4-N-CBZ-AMINOCYCLOHEXANOL trans-4-(Cbz-amino)cyclohexan-1-ol trans-4-(Cbz-aMino)cyclohexan-1-ol TRANS-4-HYDROXY-N-Z-CYCLOHEXYLAMINE trans-1-Cbz-amino-4-hydroxycyclohexane benzyl (trans-4-hydroxycyclohexyl)carbamate Benzyl (trans-4-hydroxycyclohexyl)carbaMate |
| CAS | 27489-63-0 |
| InChI | InChI=1/C14H19NO3/c16-13-8-6-12(7-9-13)15-14(17)18-10-11-4-2-1-3-5-11/h1-5,12-13,16H,6-10H2,(H,15,17)/t12-,13- |
27489-63-0 - Physico-chemical Properties
| Molecular Formula | C14H19NO3 |
| Molar Mass | 249.31 |
| Density | 1.17±0.1 g/cm3(Predicted) |
| Boling Point | 427.6±44.0 °C(Predicted) |
| Flash Point | 212.4°C |
| Vapor Presure | 4.51E-08mmHg at 25°C |
| pKa | 12.15±0.40(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.56 |
27489-63-0 - Introduction
benzyl (trans-4-hydroxycyclohexyl)carbamate, also known as benzyl (trans-4-hydroxycyclohexyl)carbamate. It is an organic compound with the chemical formula C15H19NO3.
Nature:
benzyl (trans-4-hydroxycyclohexyl)carbamate is a white crystalline solid. It is stable at room temperature and has good solubility in solvents. It is an ester compound with substitution of a benzoyl group (Cbz group) and a hydroxyl group (alcohol group). The high structural stability of this compound makes it widely used in organic synthesis.
Use:
benzyl (trans-4-hydroxycyclohexyl)carbamate is a common intermediate in organic chemical synthesis. It can be used to synthesize compounds containing Cbz-amino groups, such as drugs, pesticides, dyes and photosensitive materials. It can also be used as a temporary protecting group to protect the hydroxyl function.
Method:
benzyl (trans-4-hydroxycyclohexyl)carbamate is mainly prepared by reacting cyclohexanone with the corresponding amine compound (such as benzyl carbamate) under appropriate reaction conditions. This process usually requires a combination of solvent and catalyst to facilitate the reaction.
Safety Information:
benzyl (trans-4-hydroxycyclohexyl)carbamate has low toxicity under normal use conditions. However, as a chemical substance, care should be taken to comply with laboratory safety procedures, avoid contact with skin and eyes, and ensure that the operation is carried out in a well-ventilated environment. If accidental contact or misuse occurs, seek medical help immediately.
Nature:
benzyl (trans-4-hydroxycyclohexyl)carbamate is a white crystalline solid. It is stable at room temperature and has good solubility in solvents. It is an ester compound with substitution of a benzoyl group (Cbz group) and a hydroxyl group (alcohol group). The high structural stability of this compound makes it widely used in organic synthesis.
Use:
benzyl (trans-4-hydroxycyclohexyl)carbamate is a common intermediate in organic chemical synthesis. It can be used to synthesize compounds containing Cbz-amino groups, such as drugs, pesticides, dyes and photosensitive materials. It can also be used as a temporary protecting group to protect the hydroxyl function.
Method:
benzyl (trans-4-hydroxycyclohexyl)carbamate is mainly prepared by reacting cyclohexanone with the corresponding amine compound (such as benzyl carbamate) under appropriate reaction conditions. This process usually requires a combination of solvent and catalyst to facilitate the reaction.
Safety Information:
benzyl (trans-4-hydroxycyclohexyl)carbamate has low toxicity under normal use conditions. However, as a chemical substance, care should be taken to comply with laboratory safety procedures, avoid contact with skin and eyes, and ensure that the operation is carried out in a well-ventilated environment. If accidental contact or misuse occurs, seek medical help immediately.
Last Update：2024-04-09 15:17:56
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