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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, 2,3,5-trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-6-hydroxy-

Clc1cc(NC(=O)c2c(O)c(Cl)cc(c2Cl)Cl)c(c(c1)Cl)O Request for Quotation
Chemical Name: Benzamide, 2,3,5-trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-6-hydroxy-
CAS Number: 2277-92-1
Product Number: AG00I4HD(AGN-PC-0JKD34)
Synonyms:
MDL No:
Molecular Formula: C13H6Cl5NO3
Molecular Weight: 401.4566

Identification/Properties

Computed Properties
Molecular Weight:
401.445g/mol
XLogP3:
5.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
400.876g/mol
Monoisotopic Mass:
398.879g/mol
Topological Polar Surface Area:
69.6A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
415
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:
Danger
UN#:
3077
Hazard Statements:
H302-H410
Precautionary Statements:
P273
Class:
9
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2,3,5-Trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-6-hydroxybenzamide plays a crucial role in chemical synthesis as a versatile building block for various organic reactions. With its unique structure containing multiple chloro and hydroxy substituents on a benzamide scaffold, this compound offers a wide range of reactivity and functional group compatibility. In synthetic chemistry, it serves as a valuable intermediate for the preparation of complex molecules and pharmaceutical compounds. Its ability to participate in nucleophilic substitution, condensation, and oxidation reactions makes it a valuable tool for creating diverse chemical structures with specific properties. Designed for precision and efficiency, this compound empowers chemists to explore novel pathways in synthetic methodologies and expedite the discovery of new materials and bioactive compounds.