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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)-

Ethanone, 1-(2,3,4-trimethoxyphenyl)-

COc1ccc(c(c1OC)OC)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-(2,3,4-trimethoxyphenyl)-
CAS Number: 13909-73-4
Product Number: AG001A98(AGN-PC-0JLUSD)
Synonyms:
MDL No:
Molecular Formula: C11H14O4
Molecular Weight: 210.2265

Identification/Properties

Properties
MP:
14-15 °C(lit.)
BP:
296°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.5384(lit.)
Computed Properties
Molecular Weight:
210.229g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
210.089g/mol
Monoisotopic Mass:
210.089g/mol
Topological Polar Surface Area:
44.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
217
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
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2',3',4'-Trimethoxyacetophenone, a key aromatic compound widely utilized in chemical synthesis, plays a crucial role as a versatile building block in various organic reactions. Its unique structure, characterized by the presence of three methoxy groups, imparts distinctive chemical reactivity and properties essential for the efficient preparation of complex molecules. In chemical synthesis, 2',3',4'-Trimethoxyacetophenone exhibits remarkable utility as a precursor for the synthesis of diverse organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its functional groups serve as crucial sites for selective chemical modifications, enabling the structural diversification of molecules through various synthetic pathways. By leveraging the reactivity of the methoxy groups, chemists can introduce specific functional groups or manipulate the aromatic ring to construct intricate molecular frameworks with tailored properties and functionalities.Furthermore, 2',3',4'-Trimethoxyacetophenone's compatibility with a wide range of synthetic methodologies, such as Friedel-Crafts acylation, nucleophilic substitution, and oxidation reactions, enhances its versatility in addressing the synthetic challenges encountered in complex molecule design. The strategic incorporation of this compound in synthetic routes not only facilitates the assembly of target molecules but also allows for the exploration of novel chemical transformations and innovative synthetic strategies.Overall, the application of 2',3',4'-Trimethoxyacetophenone in chemical synthesis embodies its significance as a valuable building block for the construction of diverse organic molecules with tailored structures and functionalities. Its versatility, reactivity, and compatibility with various synthetic techniques make it an indispensable component in the toolkit of synthetic chemists seeking to unlock new opportunities in molecular design and synthesis.