N-BETA-(9-FLUORENYLMETHOXYCARBONYL)-L-HOMO(2-METHYLPHENYL)ALANINE
Fmoc-(S)-3-Amino-4-(2-methyl-phenyl)-butyric acid
CAS: 270062-91-4
Molecular Formula: C26H25NO4
N-BETA-(9-FLUORENYLMETHOXYCARBONYL)-L-HOMO(2-METHYLPHENYL)ALANINE - Names and Identifiers
N-BETA-(9-FLUORENYLMETHOXYCARBONYL)-L-HOMO(2-METHYLPHENYL)ALANINE - Physico-chemical Properties
| Molecular Formula | C26H25NO4 |
| Molar Mass | 415.48 |
| Storage Condition | Sealed in dry,2-8°C |
N-BETA-(9-FLUORENYLMETHOXYCARBONYL)-L-HOMO(2-METHYLPHENYL)ALANINE - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 10 |
| Hazard Class | IRRITANT |
N-BETA-(9-FLUORENYLMETHOXYCARBONYL)-L-HOMO(2-METHYLPHENYL)ALANINE - 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.
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
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Product Name: (S)-3-(Fmoc-Amino)-4-(2-Methylphenyl)Butyric Acid Visit Supplier Webpage Request for quotation
CAS: 270062-91-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 270062-91-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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