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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)-

Benzenesulfonamide, 5-amino-2-chloro-

Nc1ccc(c(c1)S(=O)(=O)N)Cl Request for Quotation
Chemical Name: Benzenesulfonamide, 5-amino-2-chloro-
CAS Number: 2015-19-2
Product Number: AG002DGW(AGN-PC-0JLBVM)
Synonyms:
MDL No:
Molecular Formula: C6H7ClN2O2S
Molecular Weight: 206.6500

Identification/Properties

Computed Properties
Molecular Weight:
206.644g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
205.992g/mol
Monoisotopic Mass:
205.992g/mol
Topological Polar Surface Area:
94.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
249
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-Amino-2-chlorobenzenesulfonamide, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique chemical properties make it suitable for a variety of applications in organic synthesis. Due to its amino and sulfonamide functional groups, $name$ can be used as a starting material for the synthesis of various biologically active compounds, such as pharmaceuticals and agrochemicals. Additionally, its chlorine substituent can serve as a reactive site for further functionalization, allowing for the creation of more complex molecules. Overall, the use of 5-Amino-2-chlorobenzenesulfonamide in chemical synthesis enables the development of diverse and valuable compounds with potential applications in different industries.