1,1-DIMETHYLETHYL [(1R)-2-AMINO-1-(PHENYLMETHYL)ETHYL]CARBAMATE
(R)-2-(Boc-amino)-3-phenylpropylamine
CAS: 185384-16-1
Molecular Formula: C14H22N2O2
1,1-DIMETHYLETHYL [(1R)-2-AMINO-1-(PHENYLMETHYL)ETHYL]CARBAMATE - Names and Identifiers
1,1-DIMETHYLETHYL [(1R)-2-AMINO-1-(PHENYLMETHYL)ETHYL]CARBAMATE - Physico-chemical Properties
| Molecular Formula | C14H22N2O2 |
| Molar Mass | 250.34 |
1,1-DIMETHYLETHYL [(1R)-2-AMINO-1-(PHENYLMETHYL)ETHYL]CARBAMATE - Introduction
(R)-2-(Boc-amino)-3-phenylprodrug is an organic compound with the following properties:
1. Appearance: White crystalline solid.
2. Molecular formula: C16H24N2O2.
3. Molecular weight: 276.38g/mol.
(R)-2-(Boc-amino)-3-phenylprodrug uses:
The compound is commonly used as a reagent and intermediate in organic synthesis, mainly for the synthesis of drugs and bioactive molecules.
Preparation of (R)-2-(Boc-amino)-3-phenylprodrug:
There are many ways to synthesize this compound. The most common method is to react benzaldehyde with Boc-aminopropylamine, and then perform reduction and protecting group removal reactions, and finally obtain the target product.
Safety information for (R)-2-(Boc-amino)-3-phenylamine:
This compound is generally considered to be low-toxic, but it is still necessary to pay attention to safe operation. Avoid direct contact with eyes, skin and respiratory tract when touching or using. Appropriate protective gloves and eye/face protection should be worn. Good ventilation should be ensured during use and laboratory safety practices should be observed. In case of accidental exposure or inhalation, seek medical attention promptly.
1. Appearance: White crystalline solid.
2. Molecular formula: C16H24N2O2.
3. Molecular weight: 276.38g/mol.
(R)-2-(Boc-amino)-3-phenylprodrug uses:
The compound is commonly used as a reagent and intermediate in organic synthesis, mainly for the synthesis of drugs and bioactive molecules.
Preparation of (R)-2-(Boc-amino)-3-phenylprodrug:
There are many ways to synthesize this compound. The most common method is to react benzaldehyde with Boc-aminopropylamine, and then perform reduction and protecting group removal reactions, and finally obtain the target product.
Safety information for (R)-2-(Boc-amino)-3-phenylamine:
This compound is generally considered to be low-toxic, but it is still necessary to pay attention to safe operation. Avoid direct contact with eyes, skin and respiratory tract when touching or using. Appropriate protective gloves and eye/face protection should be worn. Good ventilation should be ensured during use and laboratory safety practices should be observed. In case of accidental exposure or inhalation, seek medical attention promptly.
Last Update：2024-04-09 19:05:47
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