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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, 2-chloro-5-nitro-

[O-][N+](=O)c1ccc(c(c1)S(=O)(=O)N)Cl Request for Quotation
Chemical Name: Benzenesulfonamide, 2-chloro-5-nitro-
CAS Number: 96-72-0
Product Number: AG006OZI(AGN-PC-0JL7E6)
Synonyms:
MDL No:
Molecular Formula: C6H5ClN2O4S
Molecular Weight: 236.6329

Identification/Properties

Properties
MP:
180-183 °C
BP:
435.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
236.626g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
235.966g/mol
Monoisotopic Mass:
235.966g/mol
Topological Polar Surface Area:
114A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
320
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


2-Chloro-5-nitrobenzenesulfonamide is a versatile compound commonly used in chemical synthesis as a key building block in the production of various pharmaceuticals, and agrochemicals. With its unique chemical properties, this compound serves as a crucial intermediate in the synthesis of organic molecules with diverse applications.In organic chemistry, 2-Chloro-5-nitrobenzenesulfonamide is utilized for the preparation of sulfonamides, a class of compounds known for their antibacterial and antifungal properties. By reacting with different functional groups and reagents, this compound can undergo various chemical transformations, enabling the synthesis of complex molecules with specific biological activities.Furthermore, 2-Chloro-5-nitrobenzenesulfonamide plays a vital role in the development of pharmaceuticals due to its ability to introduce the sulfonamide group into drug candidates. This functional group is known to enhance the pharmacological properties of a compound, such as increasing its solubility, stability, and target specificity, making it a valuable tool in drug discovery and development.Additionally, in agrochemical synthesis, 2-Chloro-5-nitrobenzenesulfonamide is used for creating pesticides and herbicides with improved efficacy and selectivity. Its structural versatility allows for the modification of chemical structures to tailor the activity of the final product, making it an essential component in the production of crop protection agents.Overall, the application of 2-Chloro-5-nitrobenzenesulfonamide in chemical synthesis demonstrates its significance in the creation of innovative compounds with therapeutic and agricultural benefits.