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Fmoc-(S)-2-amino-hept-6-ynoic acid is a specialty chemical compound that is widely utilized in the realm of organic chemistry, particularly for peptide synthesis. It is characterized by the presence of an Fmoc (9-fluorenylmethoxycarbonyl) group, which acts as a protective group for the amine functionality during the synthesis process. This protective group is removed under basic conditions once the desired reaction is achieved. Additionally, the compound features an (S)-2-amino-hept-6-ynoic acid, a non-proteinogenic amino acid with a seven-carbon chain that includes an alkyne (carbon-carbon triple bond). This distinctive structure offers a high degree of versatility in research applications, such as click chemistry reactions or the synthesis of bioactive peptides. The synthesis and applications of Fmoc-(S)-2-amino-hept-6-ynoic acid are often complex and specialized, requiring a deep understanding of organic chemistry.

1097192-05-6

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1097192-05-6 Usage

Uses

Used in Organic Chemistry Research:
Fmoc-(S)-2-amino-hept-6-ynoic acid is used as a key intermediate in the synthesis of complex organic molecules, particularly in the field of peptide chemistry. Its unique structure allows for the incorporation of novel functionalities and the exploration of new synthetic pathways.
Used in Peptide Synthesis:
Fmoc-(S)-2-amino-hept-6-ynoic acid is employed as a building block in the construction of peptides, providing a versatile platform for the development of bioactive molecules with potential applications in pharmaceuticals and biotechnology.
Used in Click Chemistry:
The alkyne functionality present in Fmoc-(S)-2-amino-hept-6-ynoic acid makes it a valuable component in click chemistry reactions, a set of powerful and efficient reactions that enable the rapid and selective formation of new chemical bonds. This application is particularly useful in the synthesis of complex molecular structures and the development of new materials.
Used in Drug Discovery:
Fmoc-(S)-2-amino-hept-6-ynoic acid is used as a component in the design and synthesis of novel drug candidates, leveraging its unique structural features to create molecules with potential therapeutic properties. Its versatility in peptide synthesis and click chemistry reactions allows for the exploration of new drug targets and mechanisms of action.
Used in Materials Science:
The incorporation of Fmoc-(S)-2-amino-hept-6-ynoic acid into the synthesis of new materials can lead to the development of advanced materials with unique properties, such as improved mechanical strength, enhanced catalytic activity, or novel optical characteristics. This application can have implications in various industries, including electronics, energy, and environmental protection.

Check Digit Verification of cas no

The CAS Registry Mumber 1097192-05-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,1,9 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1097192-05:
(9*1)+(8*0)+(7*9)+(6*7)+(5*1)+(4*9)+(3*2)+(2*0)+(1*5)=166
166 % 10 = 6
So 1097192-05-6 is a valid CAS Registry Number.

1097192-05-6Downstream Products

1097192-05-6Relevant articles and documents

Nα-Fmoc-protected ω-azido- and ω-alkynyl-L- amino acids as building blocks for the synthesis of "clickable" peptides

Isaad, Alexandra Le Chevalier,Barbetti, Francesca,Rovero, Paolo,D'Ursi, Anna Maria,Chelli, Mario,Chorev, Michael,Papini, Anna Maria

experimental part, p. 5308 - 5314 (2009/06/18)

The growing interest in the 1,4-disubstituted-1,2,3-triazolyl moiety as an amide bond surrogate and its formation through very mild, chemoselective, and bioorthogonal CuI-catalyzed Huisgen 1,3-dipolar [3+2] cycloaddition of an alkynyl to an azi

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