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Catalog Number:
03709
CAS Number:
340187-12-4
Bromuro de fmoc-2-aminoetilo
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-1-amino-2-bromoetano, Fmoc-2-bromoetilamina
Documents
$29.34 /1G
Tamaño
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Product Information

Fmoc-2-aminoethylbromide is a versatile reagent widely utilized in peptide synthesis and organic chemistry. This compound features the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure allows for easy cleavage under mild conditions, making it an ideal choice for researchers looking to streamline their synthesis processes. Fmoc-2-aminoethylbromide is particularly valuable in the development of peptide-based therapeutics and in the study of protein interactions, where precise control over amino acid sequences is crucial.

In addition to its applications in peptide synthesis, Fmoc-2-aminoethylbromide is also employed in the preparation of functionalized materials and in the development of drug delivery systems. Its ability to introduce a bromoethyl group enhances the reactivity of the resulting peptides, allowing for further modifications and conjugations. This compound stands out for its efficiency and reliability, making it a preferred choice for both academic and industrial researchers focused on advancing peptide chemistry and related fields.

Synonyms
Fmoc-1-amino-2-bromoetano, Fmoc-2-bromoetilamina
CAS Number
340187-12-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C17H16NO2Br
Molecular Weight
346.2
MDL Number
MFCD00797866
PubChem ID
2759174
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-1-amino-2-bromoetano, Fmoc-2-bromoetilamina
CAS Number
340187-12-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C17H16NO2Br
Molecular Weight
346.2
MDL Number
MFCD00797866
PubChem ID
2759174
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-2-aminoethylbromide is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides. Its Fmoc (fluorenylmethyloxycarbonyl) group allows for easy protection and deprotection during the synthesis process, making it invaluable for chemists working in peptide research.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs. The ability to modify the amino acid sequence with this compound can lead to the development of novel therapeutics with improved efficacy and specificity.
  • Bioconjugation: Fmoc-2-aminoethylbromide can be employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules. This is particularly useful in creating targeted drug delivery systems.
  • Protein Engineering: It aids in the modification of proteins to enhance their stability or activity. By incorporating this compound, scientists can create proteins with tailored properties for various applications, including industrial enzymes and therapeutic proteins.
  • Diagnostic Applications: The compound is also used in developing diagnostic tools, such as biosensors. Its ability to form stable conjugates with biomolecules can improve the sensitivity and specificity of detection methods.

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