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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)-

1-Naphthalenesulfonic acid, 5-[[2-[(iodoacetyl)amino]ethyl]amino]-

ICC(=O)NCCNc1cccc2c1cccc2S(=O)(=O)O Request for Quotation
Chemical Name: 1-Naphthalenesulfonic acid, 5-[[2-[(iodoacetyl)amino]ethyl]amino]-
CAS Number: 36930-63-9
Product Number: AG00BXX9(AGN-PC-0JLZ8P)
Synonyms:
MDL No:
Molecular Formula: C14H15IN2O4S
Molecular Weight: 434.24937

Identification/Properties

Properties
MP:
>180°C (dec.)
Storage:
2-8℃;Light sensitive;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
434.248g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
433.98g/mol
Monoisotopic Mass:
433.98g/mol
Topological Polar Surface Area:
104A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
480
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


5-((2-(2-Iodoacetamido)ethyl)amino)naphthalene-1-sulfonic acid is a versatile compound frequently used in chemical synthesis procedures. This compound serves as a crucial reagent in the creation of sulfonamide derivatives, a class of compounds valued for their various biological activities and applications. In particular, the sulfonic acid group enables efficient sulfonamide bond formation, a key step in developing pharmaceuticals, agrochemicals, and materials with tailored properties. Its ability to selectively react with amines makes it an essential tool in constructing complex molecular structures with precision. Additionally, the presence of the iodoacetamido moiety offers the potential for further functionalization via cross-coupling reactions, expanding the scope of synthetic possibilities. This compound's utility in chemical synthesis extends to academic research, industrial processes, and drug discovery efforts, highlighting its significance in advancing scientific knowledge and technological innovation.