N-(9-Fluorenylmethoxycarbonyl)-1,2,3,4-tetrahydro-1-naphthylamine-4-carboxylic acid
N-(9-Fluorenylmethoxycarbonyl)-1,2,3,4-tetrahydro-1-naphthylamine-4-carboxylic acid
CAS: 1221792-81-9
Molecular Formula: C26H23NO4
N-(9-Fluorenylmethoxycarbonyl)-1,2,3,4-tetrahydro-1-naphthylamine-4-carboxylic acid - Names and Identifiers
N-(9-Fluorenylmethoxycarbonyl)-1,2,3,4-tetrahydro-1-naphthylamine-4-carboxylic acid - Physico-chemical Properties
| Molecular Formula | C26H23NO4 |
| Molar Mass | 413.47 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD16140289 |
N-(9-Fluorenylmethoxycarbonyl)-1,2,3,4-tetrahydro-1-naphthylamine-4-carboxylic acid - Risk and Safety
| Hazard Class | IRRITANT |
N-(9-Fluorenylmethoxycarbonyl)-1,2,3,4-tetrahydro-1-naphthylamine-4-carboxylic acid - Introduction
N-(a)-1,2,3, acid is an organic compound, often abbreviated as Fmoc-TNBA.
Nature:
A Fmoc-TNBA is a solid with a white or white-like color. It is stable at room temperature and soluble in some organic solvents, such as dimethyl sulfoxide (DMSO) and dimethyl formamide (DMF).
Use:
Fmoc-TNBA is a commonly used amino acid protecting group. It is frequently used for the synthesis of polypeptides and proteins and has important applications in solid phase synthesis. It can construct polypeptide chains by coupling Fmoc-TNBA with other amino acid residues. In addition, Fmoc-TNBA can also be used in the field of drug discovery and biological research.
Preparation Method:
The preparation of Fmoc-TNBA usually takes place in the organic chemistry laboratory and is obtained through multi-step synthetic reactions. Specific synthetic methods may vary depending on laboratory and research conditions.
Safety Information:
Fmoc-TNBA safety information is limited, but as a laboratory compound, the appropriate safety procedures should be followed. During operation, wear appropriate protective equipment and operate in a well-ventilated environment. In addition, attention needs to be paid to its potential irritation and possible effects on the skin, eyes and respiratory tract. Relevant regulations and laboratory safety guidelines should be observed when using and handling the compound. If detailed safety data is required, please refer to the Chemical Safety Data Sheet (SDS) or consult a relevant professional.
Nature:
A Fmoc-TNBA is a solid with a white or white-like color. It is stable at room temperature and soluble in some organic solvents, such as dimethyl sulfoxide (DMSO) and dimethyl formamide (DMF).
Use:
Fmoc-TNBA is a commonly used amino acid protecting group. It is frequently used for the synthesis of polypeptides and proteins and has important applications in solid phase synthesis. It can construct polypeptide chains by coupling Fmoc-TNBA with other amino acid residues. In addition, Fmoc-TNBA can also be used in the field of drug discovery and biological research.
Preparation Method:
The preparation of Fmoc-TNBA usually takes place in the organic chemistry laboratory and is obtained through multi-step synthetic reactions. Specific synthetic methods may vary depending on laboratory and research conditions.
Safety Information:
Fmoc-TNBA safety information is limited, but as a laboratory compound, the appropriate safety procedures should be followed. During operation, wear appropriate protective equipment and operate in a well-ventilated environment. In addition, attention needs to be paid to its potential irritation and possible effects on the skin, eyes and respiratory tract. Relevant regulations and laboratory safety guidelines should be observed when using and handling the compound. If detailed safety data is required, please refer to the Chemical Safety Data Sheet (SDS) or consult a relevant professional.
Last Update：2024-04-09 19:06:01
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