DACN(Tos,Ns) - CAS 1797508-58-7

DACN(Tos,Ns) - CAS 1797508-58-7 Catalog number: BADC-01834

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DACN(Tos,Ns) is a click chemistry reagent containing an cyclic alkyne group.

Category
ADCs Linker
Product Name
DACN(Tos,Ns)
CAS
1797508-58-7
Catalog Number
BADC-01834
Molecular Formula
C20H21N3O6S2
Molecular Weight
463.53

Ordering Information

Catalog Number Size Price Quantity
BADC-01834 -- $--
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Description
DACN(Tos,Ns) is a click chemistry reagent containing an cyclic alkyne group.
Synonyms
N-(o-nitrobenzenesulfonyl)-N'-(p-toluenesulfonyl)-4,8-diazacyclononyne
IUPAC Name
1-(4-methylphenyl)sulfonyl-5-(2-nitrophenyl)sulfonyl-1,5-diazacyclonon-7-yne
Canonical SMILES
CC1=CC=C(C=C1)S(=O)(=O)N2CCCN(CC#CC2)S(=O)(=O)C3=CC=CC=C3[N+](=O)[O-]
InChI
InChI=1S/C20H21N3O6S2/c1-17-9-11-18(12-10-17)30(26,27)21-13-4-5-14-22(16-6-15-21)31(28,29)20-8-3-2-7-19(20)23(24)25/h2-3,7-12H,6,13-16H2,1H3
InChIKey
XYCTXUMNSSJWLT-UHFFFAOYSA-N

DACN(TosNs), a versatile chemical reagent utilized in organic synthesis and biochemical research, offers a wide array of applications. Here are four key applications of DACN(TosNs)

Peptide Synthesis: A cornerstone of DACN(TosNs) application lies in peptide synthesis, where its ability to shield amino groups enables precise deprotection and coupling of amino acids, yielding intricate peptide sequences with exceptional efficiency. Researchers heavily rely on this reagent for crafting complex peptides essential for biological investigations and therapeutic advancements.

Protein Modification: Within the realm of biochemical exploration, DACN(TosNs) shines in protein modification by selectively labeling specific amino groups. This targeted alteration facilitates in-depth analysis of protein interactions, localization, and cellular functions. Notably, it aids in generating fluorescently labeled proteins crucial for imaging and tracking studies with remarkable precision.

Organic Chemistry Reactions: DACN(TosNs) stands as a pivotal tool in diverse organic synthesis reactions encompassing nucleophilic substitution and addition reactions. Its proficiency in creating stable intermediates elevates its significance in synthesizing intricate organic compounds spanning from pharmaceuticals to fine chemicals. Chemists leverage its capabilities to streamline synthetic pathways and attain pristine end products of superior purity.

Drug Development: Pharmaceutical innovators wield DACN(TosNs) in the pursuit of novel drug candidates, modifying lead compounds to optimize their pharmacological profiles. By safeguarding specific functional groups, this reagent enables strategic modifications that refine drug efficacy, stability, and safety profiles, critical in the iterative journey of drug discovery and enhancement.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Historical Records: 10-Undecynoyl-OSu | DACN(Tos,Ns)
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