N-(9-FLUORENYLMETHOXYCARBONYL)-(S)-3-AMINO-4-(2-METHYLPHENYL)BUTANOIC ACID - Names and Identifiers
N-(9-FLUORENYLMETHOXYCARBONYL)-(S)-3-AMINO-4-(2-METHYLPHENYL)BUTANOIC ACID - Physico-chemical Properties
Molecular Formula | C26H25NO4
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Molar Mass | 415.48 |
Storage Condition | Sealed in dry,2-8°C |
N-(9-FLUORENYLMETHOXYCARBONYL)-(S)-3-AMINO-4-(2-METHYLPHENYL)BUTANOIC ACID - Risk and Safety
Safety Description | S22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
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WGK Germany | 3 |
FLUKA BRAND F CODES | 10 |
Hazard Class | IRRITANT |
N-(9-FLUORENYLMETHOXYCARBONYL)-(S)-3-AMINO-4-(2-METHYLPHENYL)BUTANOIC ACID - Introduction
Fmoc-(S)-3-Amino-4-(2-methyl-phenyl)-butyric is an organic compound containing Fmoc protecting group, amino group and 2-methylphenyl group in its chemical structure. Its chemical formula is C22H21NO3.
Fmoc-(S)-3-Amino-4-(2-methyl-phenyl)-butyric acid is mainly used in peptide synthesis and solid phase synthesis in organic synthesis. It can be used as an amino acid protecting group to synthesize peptide chains by protecting the carboxyl group. In addition, it can also be used in synthetic drugs, biochemical research and protein engineering.
Fmoc-(S)-3-Amino-4-(2-methyl-phenyl)-butyric acid is usually obtained by chemical reaction of existing compounds. The specific synthesis method can vary according to the laboratory conditions and requirements, and the common synthesis methods include organic synthesis reaction and active esterification reaction.
Regarding safety information, the use of Fmoc-(S)-3-Amino-4-(2-methyl-phenyl)-butyric acid requires compliance with laboratory safety practices. Avoid contact with skin, eyes and clothing during handling and storage. Wear appropriate personal protective equipment to protect safety. The use of any chemical requires care to comply with relevant regulations and standards and to operate in the right environment.
Last Update:2024-04-09 20:02:46