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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)-

Benzenesulfonic acid, 2-amino-5-chloro-

Clc1ccc(c(c1)S(=O)(=O)O)N Request for Quotation
Chemical Name: Benzenesulfonic acid, 2-amino-5-chloro-
CAS Number: 133-74-4
Product Number: AG0011I6(AGN-PC-0JK8N6)
Synonyms:
MDL No:
Molecular Formula: C6H6ClNO3S
Molecular Weight: 207.6347

Identification/Properties

Computed Properties
Molecular Weight:
207.628g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
206.976g/mol
Monoisotopic Mass:
206.976g/mol
Topological Polar Surface Area:
88.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
248
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-5-chlorobenzenesulfonic acid, also known as ACBS, is a versatile chemical compound widely utilized in chemical synthesis applications. Its unique structure and properties make it a valuable reagent in various processes.In chemical synthesis, 2-Amino-5-chlorobenzenesulfonic acid primarily functions as a key intermediate in the production of dyes and pigments. Its sulfonic acid group is often used as a reactive site for introducing additional functional groups, allowing for the modification and optimization of dye molecules. This compound's ability to undergo various chemical reactions, such as diazotization and coupling reactions, enables the synthesis of a diverse range of colored compounds with specific properties.Furthermore, 2-Amino-5-chlorobenzenesulfonic acid plays a crucial role in the development of pharmaceuticals and agrochemicals. Its presence in synthesis pathways can lead to the creation of biologically active molecules with targeted functions. By incorporating this compound into the design of new chemical entities, researchers can explore novel applications and potentially discover compounds with enhanced therapeutic or agricultural properties.Overall, 2-Amino-5-chlorobenzenesulfonic acid's importance in chemical synthesis lies in its versatility and reactivity, making it a valuable building block for creating complex molecules in various industries.