83303-83-7 Usage
Molecular Structure
1-methoxy-4-[2-(4-methoxyphenyl)pent-1-en-3-yl]benzene consists of a benzene ring with a methoxy group at the 1-position and a long chain aliphatic group at the 4-position, which contains a double bond and is attached to a phenyl ring with a methoxy group at the 4-position.
Aromatic Properties
The compound has aromatic properties due to the presence of the benzene ring, which contributes to its use in the fragrance industry.
Reactivity
The presence of the double bond in the aliphatic group and the methoxy groups on the phenyl rings make the compound reactive and useful in the production of organic compounds and pharmaceuticals.
Medicinal Applications
1-methoxy-4-[2-(4-methoxyphenyl)pent-1-en-3-yl]benzene has potential medicinal applications and is being studied for its pharmaceutical properties.
Usage
The compound is commonly used in the production of organic compounds, pharmaceuticals, and fragrances.
Check Digit Verification of cas no
The CAS Registry Mumber 83303-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,0 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83303-83:
(7*8)+(6*3)+(5*3)+(4*0)+(3*3)+(2*8)+(1*3)=117
117 % 10 = 7
So 83303-83-7 is a valid CAS Registry Number.
83303-83-7Relevant academic research and scientific papers
Nonsteroidal Estrogens: Synthesis and Estrogen Receptor Binding Affinity of Derivatives of (3R*,4S*)-3,4-Bis(4-hydroxyphenyl)hexane (Hexestrol) and (2R*,3S*)-2,3-Bis(4-hydroxyphenyl)pentane (Norhexestrol) Functionalized on the Side Chain
Landvatter, Scott W.,Katzenellenbogen, John A.
, p. 1300 - 1307 (2007/10/02)
A series of nonsteroidal, side-chain functionalized estrogens based on (3R*,4S*)-3,4-bis(4-hydroxyphenyl)hexane (hexestrol) and (2R*,3S*)-2,3-bis(4-hydroxyphenyl)pentane (norhexestrol) has been prepared; these include amide, diazo ketone, ester, alcohol, ketone, fluoro,bromo, iodo, and saturated hydrocarbon derivatives.Analysis of the binding affinity of these compounds to the uterine estrogen receptor, measured by competitive binding assay, reveals trends that can be related to the steric size, the hydrophobicity, and the hydrogen bond accepting character of the side-chain substituents.Comparison of binding affinities between norhexestrol and hexestrol derivatives indicates that, in general, the norhexestrols show significantly higher receptor binding affinities, making this series of compounds ideally suited as functional probes for the estrogen receptor.
