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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,5-(aminosulfonyl)-4-chloro-N-(2,6-dimethylphenyl)-2-hydroxy-

O=C(c1cc(c(cc1O)Cl)S(=O)(=O)N)Nc1c(C)cccc1C Request for Quotation
Chemical Name: Benzamide,5-(aminosulfonyl)-4-chloro-N-(2,6-dimethylphenyl)-2-hydroxy-
CAS Number: 14293-44-8
Product Number: AG00HWQR(AGN-PC-0PT6TW)
Synonyms:
MDL No:
Molecular Formula: C15H15ClN2O4S
Molecular Weight: 354.8086

Identification/Properties

Computed Properties
Molecular Weight:
354.805g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
354.044g/mol
Monoisotopic Mass:
354.044g/mol
Topological Polar Surface Area:
118A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
526
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Xipamide, a sulfonamide diuretic compound, is widely utilized in chemical synthesis as a versatile building block for pharmaceutical research and development. Its functional groups, including the sulfonamide moiety and the chloroacetamide group, enable it to participate in a variety of synthetic transformations.In organic synthesis, Xipamide can serve as a key intermediate in the preparation of various bioactive compounds and pharmaceutical agents. Its unique structural features make it an important precursor for the modification of drug candidates and the synthesis of new chemical entities with potential therapeutic applications.Furthermore, Xipamide's reactivity under different reaction conditions allows for the introduction of specific functional groups or stereochemical elements into complex molecular structures. This versatility makes it a valuable tool for medicinal chemists and researchers working on the design and synthesis of novel drug molecules.