cardamonin


Chemical Name: cardamonin
CAS Number: 19309-14-9
Product Number: AG00AOR0(AGN-PC-0WQUA8)
Synonyms:
MDL No:
Molecular Formula: C16H14O4
Molecular Weight: 270.2800

Identification/Properties


Computed Properties
Molecular Weight:
270.284g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
270.089g/mol
Monoisotopic Mass:
270.089g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
346
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


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



The compound (2E)-1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenyl-2-propen-1-one, also known as $name$, plays a crucial role in chemical synthesis as a key intermediate in the production of various pharmaceuticals and fine chemicals. This compound serves as a versatile building block due to its unique structure, which contains a conjugated enone system and functional groups such as hydroxyl and methoxy groups.In chemical synthesis, (2E)-1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenyl-2-propen-1-one is commonly utilized for the development of novel drug candidates, natural product derivatives, and bioactive molecules. Its reactive double bond allows for the introduction of different substituents through various synthetic transformations, enabling the modification of its pharmacological properties and biological activities.Furthermore, the presence of phenolic hydroxyl groups in the molecule enhances its antioxidant and radical scavenging capabilities, making it valuable for the synthesis of antioxidant agents and anti-inflammatory compounds. The methoxy group contributes to the compound's lipophilicity and can influence its bioavailability and interaction with biological targets.Overall, (2E)-1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenyl-2-propen-1-one is a versatile compound in chemical synthesis, offering diverse opportunities for designing and synthesizing novel compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.