Benzene, 1,3-dimethoxy-5-[(1Z)-2-(4-methoxyphenyl)ethenyl]-


Chemical Name: Benzene, 1,3-dimethoxy-5-[(1Z)-2-(4-methoxyphenyl)ethenyl]-
CAS Number: 94608-23-8
Product Number: AG005WAH(AGN-PC-0ONXCL)
Synonyms:
MDL No: MFCD11977725
Molecular Formula: C17H18O3
Molecular Weight: 270.3230

Identification/Properties


Computed Properties
Molecular Weight:
270.328g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
270.126g/mol
Monoisotopic Mass:
270.126g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
283
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



(Z)-3,5,4′-Trimethoxystilbene, also known as resveratrol trimethyl ether, is a valuable compound in chemical synthesis due to its unique properties and versatile applications. In organic chemistry, this compound serves as a key building block for the synthesis of various biologically active molecules and pharmaceuticals.One of the primary applications of (Z)-3,5,4′-Trimethoxystilbene is its role as a precursor in the synthesis of stilbene derivatives. By utilizing this compound as a starting material, chemists can introduce functional groups and modify the structure to create new and potent molecules with diverse properties.Additionally, (Z)-3,5,4′-Trimethoxystilbene is commonly used in the synthesis of natural product analogs and pharmaceutical agents. Its structure provides a platform for the development of novel drugs with enhanced bioactivity and pharmacokinetic profiles.Moreover, (Z)-3,5,4′-Trimethoxystilbene exhibits antioxidant and anti-inflammatory properties, making it a promising candidate for the formulation of nutraceuticals and skincare products. Its ability to scavenge free radicals and protect against oxidative stress further expands its applications in various industries.Overall, (Z)-3,5,4′-Trimethoxystilbene plays a crucial role in chemical synthesis by serving as a versatile intermediate for the construction of biologically active compounds, pharmaceuticals, and functional materials. Its wide range of applications and beneficial properties make it an indispensable component in the toolkit of synthetic chemists and researchers in the field of medicinal chemistry.