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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)-

Benzenamine, 2-methoxy-5-(4-morpholinylsulfonyl)-

COc1ccc(cc1N)S(=O)(=O)N1CCOCC1 Request for Quotation
Chemical Name: Benzenamine, 2-methoxy-5-(4-morpholinylsulfonyl)-
CAS Number: 56807-17-1
Product Number: AG00ECIB(AGN-PC-0JOGLN)
Synonyms:
MDL No:
Molecular Formula: C11H16N2O4S
Molecular Weight: 272.3207

Identification/Properties

Computed Properties
Molecular Weight:
272.319g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
272.083g/mol
Monoisotopic Mass:
272.083g/mol
Topological Polar Surface Area:
90.2A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
362
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


2-Methoxy-5-(morpholinosulfonyl)aniline, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role in organic chemistry due to its ability to serve as a key building block in the synthesis of various complex molecules.One of the primary applications of 2-Methoxy-5-(morpholinosulfonyl)aniline is as a coupling agent in peptide synthesis. Its unique structure allows for efficient and precise coupling reactions, essential for the production of peptides with high yields and purity. By acting as a coupling reagent, this compound facilitates the formation of peptide bonds and enables the synthesis of custom-designed peptides for use in biochemical research, pharmaceutical development, and other scientific applications.Additionally, 2-Methoxy-5-(morpholinosulfonyl)aniline is commonly employed in the preparation of heterocyclic compounds. Its sulfonamide group and morpholine ring make it a valuable precursor for the synthesis of various heterocycles, such as benzimidazoles, oxazoles, and thiazoles. These heterocyclic compounds are essential in drug discovery and development, as well as in the production of agrochemicals and materials science.Overall, 2-Methoxy-5-(morpholinosulfonyl)aniline is a highly versatile compound with diverse applications in chemical synthesis, particularly in peptide coupling and heterocyclic chemistry. Its unique properties make it an indispensable tool for researchers and chemists working in the fields of organic synthesis and medicinal chemistry.