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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)-

2-amino-N-ethylbenzenesulfonamide

CCNS(=O)(=O)c1ccccc1N Request for Quotation
Chemical Name: 2-amino-N-ethylbenzenesulfonamide
CAS Number: 98489-77-1
Product Number: AG006839(AGN-PC-0162SQ)
Synonyms:
MDL No:
Molecular Formula: C8H12N2O2S
Molecular Weight: 200.2581

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
200.256g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
200.062g/mol
Monoisotopic Mass:
200.062g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
245
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-N-ethylbenzenesulfonamide is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. One of the key applications of this compound is as a building block in the synthesis of various organic compounds. Due to its amino and sulfonamide functional groups, it serves as a valuable starting material for the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. In particular, the amino group can undergo various reactions such as acylation, alkylation, and condensation reactions to introduce different functional groups, allowing for the creation of diverse molecular structures. Additionally, the sulfonamide group provides stability and can participate in hydrogen bonding interactions, making it useful for designing molecules with specific biological activities. Overall, the strategic incorporation of 2-Amino-N-ethylbenzenesulfonamide in chemical synthesis facilitates the preparation of complex molecules with tailored properties for a range of applications in industry and research.