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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, 3-amino-4-chloro-

Clc1ccc(cc1N)S(=O)(=O)N Request for Quotation
Chemical Name: Benzenesulfonamide, 3-amino-4-chloro-
CAS Number: 29092-34-0
Product Number: AG002XAR(AGN-PC-0JM1HL)
Synonyms:
MDL No:
Molecular Formula: C6H7ClN2O2S
Molecular Weight: 206.6500

Identification/Properties

Computed Properties
Molecular Weight:
206.644g/mol
XLogP3:
0.9
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H312-H315-H319-H332-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-4-chlorobenzenesulfonamide, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role as a building block in the creation of various pharmaceuticals, agrochemicals, and dyes. In chemical synthesis, 3-Amino-4-chlorobenzenesulfonamide is often employed for its reactivity and functional group properties. It serves as a key intermediate in the production of sulfonamide antibiotics, which are essential in treating bacterial infections. Additionally, this compound is utilized in the synthesis of herbicides and insecticides, contributing to pest control and agriculture. Furthermore, 3-Amino-4-chlorobenzenesulfonamide is a valuable component in dye production, enabling the creation of vibrant and color-fast dyes for textiles and other materials. Its unique chemical structure allows for precise modifications, making it an important tool in the synthesis of various organic compounds. Overall, the application of 3-Amino-4-chlorobenzenesulfonamide in chemical synthesis is instrumental in the development of diverse products that benefit the pharmaceutical, agricultural, and textile industries.