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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-(3-azido-1-oxopropoxy)-

O=C(ON1C(=O)CCC1=O)CCN=[N+]=[N-] Request for Quotation
Chemical Name: 2,5-Pyrrolidinedione, 1-(3-azido-1-oxopropoxy)-
CAS Number: 850180-76-6
Product Number: AG003IYC(AGN-PC-00AN72)
Synonyms:
MDL No:
Molecular Formula: C7H8N4O4
Molecular Weight: 212.1628

Identification/Properties

Computed Properties
Molecular Weight:
212.165g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
212.055g/mol
Monoisotopic Mass:
212.055g/mol
Topological Polar Surface Area:
78A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
331
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


In chemical synthesis, 3-azidopropanoate-N-hydroxysuccinimide ester serves as a versatile reagent for bioconjugation and crosslinking reactions. This compound is commonly used in the functionalization of proteins, peptides, and other biomolecules for various analytical and research applications. By reacting with primary amines on the target molecules, 3-azidopropanoate-N-hydroxysuccinimide ester enables the introduction of azide groups, which can further participate in click chemistry reactions for site-specific labeling or immobilization purposes. Additionally, this reagent offers excellent stability and selectivity, making it a valuable tool for the controlled modification of biomolecules in complex systems.