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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)-

Acetamide, N-[4-[(4-aminophenyl)sulfonyl]phenyl]-

CC(=O)Nc1ccc(cc1)S(=O)(=O)c1ccc(cc1)N Request for Quotation
Chemical Name: Acetamide, N-[4-[(4-aminophenyl)sulfonyl]phenyl]-
CAS Number: 565-20-8
Product Number: AG00EEJF(AGN-PC-07Y468)
Synonyms:
MDL No:
Molecular Formula: C14H14N2O3S
Molecular Weight: 290.3376

Identification/Properties

Properties
MP:
>218°C (dec.)
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
290.337g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
290.073g/mol
Monoisotopic Mass:
290.073g/mol
Topological Polar Surface Area:
97.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
428
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Monoacetyldapsone is a versatile compound that finds widespread application in various chemical synthesis processes. Due to its unique structure and reactivity, Monoacetyldapsone serves as a key building block in the synthesis of complex organic molecules. Its acetyl group enables selective functionalization reactions, allowing chemists to introduce specific substituents at desired positions in target molecules. This compound is particularly valued in the pharmaceutical industry, where precise control over chemical structure is crucial for the development of new drugs. In addition, Monoacetyldapsone is utilized in the preparation of advanced materials, fine chemicals, and agrochemicals, showcasing its significance in modern synthetic chemistry. With its utility in diverse synthetic transformations, Monoacetyldapsone continues to play a pivotal role in enabling the creation of innovative compounds across various scientific disciplines.