RARECHEM AK PT F005
Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid
CAS: 270596-45-7
Molecular Formula: C27H25NO4
RARECHEM AK PT F005 - Names and Identifiers
RARECHEM AK PT F005 - Physico-chemical Properties
| Molecular Formula | C27H25NO4 |
| Molar Mass | 427.49 |
| Density | 1.240±0.06 g/cm3 (20 ºC 760 Torr) |
| Storage Condition | Sealed in dry,2-8°C |
RARECHEM AK PT F005 - 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 |
RARECHEM AK PT F005 - Introduction
Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid is an organic compound with a 6-carbon straight chain of alkenes, phenyl and amino functional groups in its chemical structure. It is a chiral compound, I .e., has a levorotatory configuration.
Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid is commonly used in peptide synthesis and solid phase synthesis. It can be used as a starting material or intermediate for the synthesis of peptide fragments and can be used to construct peptides with specific biological activities.
The method for preparing Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid can be carried out by organic synthesis methods. One common synthetic approach is to use existing compounds for functionalization reactions, such as mono-substituted olefins linked to phenylacetic acid and amination reagents. The specific synthetic steps and conditions need to refer to the relevant research literature or patent.
Regarding its safety information, Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid is a laboratory reagent and needs to be properly operated in the laboratory. Care should be taken to avoid inhalation, ingestion or skin contact during use. At the same time, it needs to be stored in a dry, cool place and avoid contact with oxidants and other substances. Please read the relevant safety information and operating instructions before use.
Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid is commonly used in peptide synthesis and solid phase synthesis. It can be used as a starting material or intermediate for the synthesis of peptide fragments and can be used to construct peptides with specific biological activities.
The method for preparing Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid can be carried out by organic synthesis methods. One common synthetic approach is to use existing compounds for functionalization reactions, such as mono-substituted olefins linked to phenylacetic acid and amination reagents. The specific synthetic steps and conditions need to refer to the relevant research literature or patent.
Regarding its safety information, Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid is a laboratory reagent and needs to be properly operated in the laboratory. Care should be taken to avoid inhalation, ingestion or skin contact during use. At the same time, it needs to be stored in a dry, cool place and avoid contact with oxidants and other substances. Please read the relevant safety information and operating instructions before use.
Last Update：2024-04-09 21:54:55
