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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, 3,5-dimethoxy-

COc1cc(OC)cc(c1)C(=O)N Request for Quotation
Chemical Name: Benzamide, 3,5-dimethoxy-
CAS Number: 17213-58-0
Product Number: AG003INT(AGN-PC-0JLAUX)
Synonyms:
MDL No:
Molecular Formula: C9H11NO3
Molecular Weight: 181.1885

Identification/Properties

Properties
MP:
145-148 °C(lit.)
BP:
285.9 °C at 760 mmHg
Form:
Solid
Computed Properties
Molecular Weight:
181.191g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
181.074g/mol
Monoisotopic Mass:
181.074g/mol
Topological Polar Surface Area:
61.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Dimethoxybenzamide is a versatile compound with significant application in chemical synthesis. As a key building block in organic chemistry, 3,5-Dimethoxybenzamide plays a crucial role in the construction of various pharmaceuticals, agrochemicals, and fine chemicals. Its primary function lies in serving as a precursor for the synthesis of complex molecules through various chemical reactions such as acylation, amidation, and nucleophilic substitution. This compound's unique structure and reactivity make it an essential reagent for producing a wide range of functionalized benzamides and related compounds with diverse biological activities. Moreover, 3,5-Dimethoxybenzamide's compatibility with different synthetic strategies and its ability to introduce specific functional groups position it as a valuable tool for the development of novel chemical entities with potential applications in medicinal chemistry and material science.