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1097192-05-6

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1097192-05-6 Usage

General Description

Fmoc-(S)-2-amino-hept-6-ynoic acid is a specialty chemical often used in the field of organic chemistry, specifically in peptide synthesis. The Fmoc (9-fluorenylmethoxycarbonyl) group is a protective group used in the synthesis of peptides, which protects the amine functionality until the desired reaction is complete before being removed under basic conditions. The (S)-2-amino-hept-6-ynoic acid is a non-proteinogenic amino acid with a seven carbon chain that contains an alkyne (carbon-carbon triple bond). This unique structure can provide versatility in research applications such as click chemistry reactions or the synthesis of bioactive peptides. Its synthesis and applications can be complex and specialized, often necessitating a strong understanding of organic chemistry.

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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