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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)-

Benzamide, N-[2-[4-(aminosulfonyl)phenyl]ethyl]-5-chloro-2-methoxy-

COc1ccc(cc1C(=O)NCCc1ccc(cc1)S(=O)(=O)N)Cl Request for Quotation
Chemical Name: Benzamide, N-[2-[4-(aminosulfonyl)phenyl]ethyl]-5-chloro-2-methoxy-
CAS Number: 16673-34-0
Product Number: AG0033VP(AGN-PC-0JLVRF)
Synonyms:
MDL No:
Molecular Formula: C16H17ClN2O4S
Molecular Weight: 368.8352

Identification/Properties

Properties
MP:
209-214 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
368.832g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
368.06g/mol
Monoisotopic Mass:
368.06g/mol
Topological Polar Surface Area:
107A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
515
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chloro-2-methoxy-N-(4-sulfamoylphenethyl)benzamide is a versatile compound that finds widespread use in chemical synthesis processes. Due to its unique structural properties, this compound serves as a valuable building block for the creation of various pharmaceutical intermediates and bioactive molecules. Its presence in the synthesis pathway allows for the introduction of specific functional groups and enhances the biological activity of the final products. In addition, the strategic incorporation of 5-Chloro-2-methoxy-N-(4-sulfamoylphenethyl)benzamide in chemical reactions facilitates the formation of complex molecular structures with improved pharmacological properties. Its role in chemical synthesis extends to the development of innovative drug candidates and research compounds in the pharmaceutical industry.