Benzene, 1,2,3,4-tetramethoxy-5-methyl-


Chemical Name: Benzene, 1,2,3,4-tetramethoxy-5-methyl-
CAS Number: 35896-58-3
Product Number: AG003FDP(AGN-PC-0MV005)
Synonyms:
MDL No:
Molecular Formula: C11H16O4
Molecular Weight: 212.2423

Identification/Properties


Properties
BP:
282.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
1.5100 to 1.5140
Computed Properties
Molecular Weight:
212.245g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
212.105g/mol
Monoisotopic Mass:
212.105g/mol
Topological Polar Surface Area:
36.9A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
185
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



1,2,3,4-Tetramethoxy-5-methylbenzene, also known as piperonal or heliotropin, serves as a valuable building block in chemical synthesis due to its versatile reactivity and unique structural properties. This compound is commonly employed in the production of fragrances, pharmaceuticals, and agrochemicals.In chemical synthesis, 1,2,3,4-Tetramethoxy-5-methylbenzene can be utilized as a precursor in the preparation of various aromatic compounds. Its methoxy groups can serve as directing or protecting groups in organic reactions, allowing for selective functionalization at specific positions on the benzene ring. Furthermore, its aldehyde functionality enables it to participate in condensation reactions, facilitating the formation of complex molecular structures.Additionally, 1,2,3,4-Tetramethoxy-5-methylbenzene can undergo oxidation reactions to yield piperonylic acid, a key intermediate in the synthesis of numerous pharmaceuticals and natural products. Its aromatic nature and electron-donating methoxy groups make it a suitable substrate for oxidative transformations, enabling the introduction of diverse functional groups into organic molecules.Overall, the strategic placement of methoxy and methyl substituents on the benzene ring of 1,2,3,4-Tetramethoxy-5-methylbenzene imparts it with remarkable synthetic utility across various industries, making it a valuable compound for the creation of novel chemical entities.