63335-23-9 Usage
Uses
Used in Pharmaceutical Industry:
1-(2,6-Dihydroxyphenyl)-9-phenyl-1-nonanone is used as an anticancer agent for its potential properties in inhibiting the growth and progression of various types of cancer. Its antioxidant and anti-inflammatory effects also contribute to its potential use in treating neurodegenerative diseases such as Alzheimer's and Parkinson's.
Used in Food Industry:
1-(2,6-Dihydroxyphenyl)-9-phenyl-1-nonanone is used as a natural food coloring agent due to its vibrant color, offering an alternative to synthetic dyes. Additionally, it has been investigated for its potential use in food preservation, enhancing the shelf life and quality of various food products.
Used in Agriculture:
1-(2,6-Dihydroxyphenyl)-9-phenyl-1-nonanone has potential applications in agriculture, particularly in the development of natural pesticides or growth promoters, leveraging its antioxidant and anti-inflammatory properties to improve crop health and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 63335-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,3 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63335-23:
(7*6)+(6*3)+(5*3)+(4*3)+(3*5)+(2*2)+(1*3)=109
109 % 10 = 9
So 63335-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H26O3/c22-18(21-19(23)15-10-16-20(21)24)14-9-4-2-1-3-6-11-17-12-7-5-8-13-17/h5,7-8,10,12-13,15-16,23-24H,1-4,6,9,11,14H2
63335-23-9Relevant academic research and scientific papers
Synthesis of 1-(2,6-Dihydroxyphenyl)-1-alkanones and benzophenone by aromatization of 2-acyl-3-hydroxy-2-cyclohexene-1-ones with mercuric acetate
Oliver,Wilzer,Waters
, p. 1117 - 1119 (2007/10/02)
1-(2,6-Dihydroxyphenyl)-1-alkanones, natural products identified from insects and from medicinal plants, are readily prepared from 1,3-cyclohexanedione and appropriate carboxylic acids. The final step involves aromatization using mercuric acetate.
Synthesis of Malabaricone-A - Confirmation of its Structure
Parthasarathy, M. R.,Gupta, Sushma
, p. 965 (2007/10/02)
Wittig reaction of 7-phenylheptyl bromide (I) with 2,6-dimethoxyphenylglyoxal (II) affords 1-(2,6-dimethoxybenzoyl)-8-phenyl-oct-1-ene (III).III on hydrogenation over Pd/C catalyst followed by demethylation with pyridine hydrobromide yields malabaricone-A
