Carbamic acid, N-[(1S)-2-iodo-1-methylethyl]-, 1,1-dimethylethyl ester
(S)-(2-Iodo-1-methyl-ethyl)-carbamic acid tert-butyl ester
CAS: 161529-20-0
Molecular Formula: C8H16INO2
Carbamic acid, N-[(1S)-2-iodo-1-methylethyl]-, 1,1-dimethylethyl ester - Names and Identifiers
Carbamic acid, N-[(1S)-2-iodo-1-methylethyl]-, 1,1-dimethylethyl ester - Physico-chemical Properties
| Molecular Formula | C8H16INO2 |
| Molar Mass | 285.12 |
| Density | 1.483±0.06 g/cm3(Predicted) |
| Melting Point | 58-60 °C |
| Boling Point | 291.6±23.0 °C(Predicted) |
| pKa | 11.85±0.46(Predicted) |
Carbamic acid, N-[(1S)-2-iodo-1-methylethyl]-, 1,1-dimethylethyl ester - Introduction
(S)-(2-Iodo-1-methyl-ethyl)-carbamic acid tert-butyl ester, also known as (S)-2-amino -1-(3,3-dimethylpropoxy) ethane, it is an organic compound. Its chemical formula is C8H16INO2.
The compound is a chiral compound with two chiral centers. Its (R)-isomer also exists. This compound usually exists in liquid form and has a colorless or light yellow appearance. It has a special smell and is soluble in many organic solvents.
(S)-(2-Iodo-1-methyl-ethyl)-carbamic acid tert-butyl ester has a wide range of applications in organic synthesis. The most common use is as an intermediate in the synthesis of other chiral compounds. It is commonly used in the synthesis of drugs, pesticides and other biologically active organic molecules.
This compound is typically formed by reacting (S)-2-amino -1-(3,3-dimethylpropoxy) ethane with hydrogen iodide.
When handling this compound, you should pay attention to the following safety information: It is an organic halogen compound, which is irritating and corrosive. During the operation, direct contact with skin and eyes should be avoided, and the operation should be carried out in a well-ventilated place. During handling and storage, relevant safety procedures should be followed and appropriate protective measures should be taken, such as wearing protective gloves, goggles and protective clothing.
The compound is a chiral compound with two chiral centers. Its (R)-isomer also exists. This compound usually exists in liquid form and has a colorless or light yellow appearance. It has a special smell and is soluble in many organic solvents.
(S)-(2-Iodo-1-methyl-ethyl)-carbamic acid tert-butyl ester has a wide range of applications in organic synthesis. The most common use is as an intermediate in the synthesis of other chiral compounds. It is commonly used in the synthesis of drugs, pesticides and other biologically active organic molecules.
This compound is typically formed by reacting (S)-2-amino -1-(3,3-dimethylpropoxy) ethane with hydrogen iodide.
When handling this compound, you should pay attention to the following safety information: It is an organic halogen compound, which is irritating and corrosive. During the operation, direct contact with skin and eyes should be avoided, and the operation should be carried out in a well-ventilated place. During handling and storage, relevant safety procedures should be followed and appropriate protective measures should be taken, such as wearing protective gloves, goggles and protective clothing.
Last Update：2024-04-09 02:00:42
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