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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, 4-amino-N-cyclopropyl-

Nc1ccc(cc1)S(=O)(=O)NC1CC1 Request for Quotation
Chemical Name: Benzenesulfonamide, 4-amino-N-cyclopropyl-
CAS Number: 177785-41-0
Product Number: AG0025JF(AGN-PC-0K0ZFR)
Synonyms:
MDL No:
Molecular Formula: C9H12N2O2S
Molecular Weight: 212.2688

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
212.267g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
212.062g/mol
Monoisotopic Mass:
212.062g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
284
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:
H302-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


N-Cyclopropyl 4-Aminophenylsulfonamide, also known as $name$, serves as a versatile building block in chemical synthesis. This compound is commonly utilized as a valuable intermediate in the production of various pharmaceuticals and agrochemicals due to its unique structural properties and functional groups. In chemical synthesis, N-Cyclopropyl 4-Aminophenylsulfonamide plays a crucial role as a key starting material for creating complex organic molecules with specific biological activities. Its cyclopropyl ring provides rigidity and sterics, influencing the overall reactivity and selectivity of reactions. Additionally, the sulfonamide and amino groups offer opportunities for diverse functionalization, enabling the synthesis of a wide range of compounds with tailored properties. This compound's importance lies in its ability to facilitate the construction of intricate molecular architectures, making it an indispensable tool in modern organic synthesis methodologies.