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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)-

Benzaldehyde, 4-methoxy-2,3,6-trimethyl-

COc1cc(C)c(c(c1C)C)C=O Request for Quotation
Chemical Name: Benzaldehyde, 4-methoxy-2,3,6-trimethyl-
CAS Number: 54344-92-2
Product Number: AG00DAWD(AGN-PC-07A22K)
Synonyms:
MDL No:
Molecular Formula: C11H14O2
Molecular Weight: 178.2277

Identification/Properties

Properties
MP:
63.0 to 68.0 °C
BP:
301.2 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
178.231g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
178.099g/mol
Monoisotopic Mass:
178.099g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
179
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methoxy-2,3,6-trimethylbenzaldehyde, also known as $name$, is a versatile compound widely utilized in various chemical synthesis processes. This aldehyde compound plays a crucial role as a building block in the creation of numerous organic compounds due to its unique structure and reactivity.One key application of $name$ in chemical synthesis is as a precursor in the synthesis of pharmaceuticals and agrochemicals. Its aromatic aldehyde group provides a distinctive functionality that can be modified and transformed into a wide range of biologically active molecules. By incorporating $name$ into the synthesis of these compounds, chemists can control the structure and properties of the final products, leading to the development of new drugs and crop protection agents.Additionally, $name$ is often employed in the preparation of fragrances and flavoring agents. Its methoxy and methyl substituents contribute to the compound's aromatic nature, making it a valuable component in the creation of pleasant scents and tastes. By incorporating $name$ into fragrance synthesis, chemists can tailor the olfactory profile of the final products, catering to specific consumer preferences.Furthermore, 4-Methoxy-2,3,6-trimethylbenzaldehyde is utilized in the production of dyes and pigments. Its unique structure allows for the modification of the aromatic ring, leading to the formation of vibrant and stable colorants. By incorporating $name$ into the synthesis of these colorants, chemists can achieve a wide range of hues and shades, making it a versatile compound in the textile and coatings industries.Overall, 4-Methoxy-2,3,6-trimethylbenzaldehyde serves as a valuable building block in chemical synthesis, enabling the creation of diverse organic compounds with applications in pharmaceuticals, fragrances, flavors, dyes, and pigments. Its versatility and reactivity make it an essential component in the toolkit of synthetic chemists striving to develop new and innovative materials.