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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2,5-Pyrrolidinedione, 1-[(4-azido-2-hydroxybenzoyl)oxy]-

[N-]=[N+]=Nc1ccc(c(c1)O)C(=O)ON1C(=O)CCC1=O Request for Quotation
Chemical Name: 2,5-Pyrrolidinedione, 1-[(4-azido-2-hydroxybenzoyl)oxy]-
CAS Number: 96602-46-9
Product Number: AG006PN3(AGN-PC-0KO7DL)
Synonyms:
MDL No:
Molecular Formula: C11H8N4O5
Molecular Weight: 276.2050

Identification/Properties

Properties
MP:
>145°C (dec.)
Storage:
-10 ℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
276.208g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
4
Exact Mass:
276.049g/mol
Monoisotopic Mass:
276.049g/mol
Topological Polar Surface Area:
98.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
471
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Succinimidyl 4-azidosalicylate is a versatile compound widely used in chemical synthesis for bioconjugation and labeling purposes. This reagent contains an azide group, which is a powerful and selective reactive moiety in click chemistry reactions. Through azide-alkyne cycloaddition reactions, N-Succinimidyl 4-azidosalicylate can efficiently and covalently attach to alkynes or other complementary functional groups, enabling the specific conjugation of biomolecules, polymers, or surfaces. Its high stability and solubility in common organic solvents make it a valuable tool for creating complex molecular architectures or designing novel materials with tailored properties. In addition, the succinimidyl group in N-Succinimidyl 4-azidosalicylate enhances the stability of the formed conjugates, ensuring long-term functionality and utility in various applications within the field of chemical synthesis.