(S)-3-(FMOC-AMINO)-6-PHENYL-5-HEXENOIC ACID
Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid
CAS: 270596-45-7
Molecular Formula: C27H25NO4
(S)-3-(FMOC-AMINO)-6-PHENYL-5-HEXENOIC ACID - Names and Identifiers
(S)-3-(FMOC-AMINO)-6-PHENYL-5-HEXENOIC ACID - 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 |
(S)-3-(FMOC-AMINO)-6-PHENYL-5-HEXENOIC ACID - 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 |
(S)-3-(FMOC-AMINO)-6-PHENYL-5-HEXENOIC ACID - 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
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Tel: +86 0512-69209928
Email: wuhao@highfine.com
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Spot supply
Product Name: Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoicacid Request for quotationCAS: 270596-45-7
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365
Wechat: 18916960931
Spot supply
Product Name: Fmoc-styryl-L-beta-homoalanine Visit Supplier Webpage Request for quotationCAS: 270596-45-7
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
WhatsApp: +86-18821248368
Product Name: Fmoc-(S)-3-Amino-(6-phenyl)-5-hexenoic acid Request for quotation
CAS: 270596-45-7
Tel: +86 0512-69209928
Email: wuhao@highfine.com
merry@highfine.com
chenmengqi@highfine.com
QQ: 4006286883
CAS: 270596-45-7
Tel: +86 0512-69209928
Email: wuhao@highfine.com
merry@highfine.com
chenmengqi@highfine.com
QQ: 4006286883
View History
(S)-3-(FMOC-AMINO)-6-PHENYL-5-HEXENOIC ACID
2-Amino-1-(3-pyridinyl)ethanol Dihydrochloride
Α,Α-二苯基-1-哌啶丙醇
AdaN-[2-Acetamido]-2-IminodiaceticAcid
(R)-(+)-ALPHA-(1-NAPHTHYL)ETHYLAMINE
2-Amino-1-(3-pyridinyl)ethanol Dihydrochloride
Α,Α-二苯基-1-哌啶丙醇
AdaN-[2-Acetamido]-2-IminodiaceticAcid
(R)-(+)-ALPHA-(1-NAPHTHYL)ETHYLAMINE