762-29-8 Usage
Description
Farnesylacetone is a naturally occurring organic compound that serves as an intermediate in the biosynthesis of carotenoids, which are pigments responsible for the vibrant colors found in many plants, fruits, and vegetables. It plays a crucial role in the formation of these essential compounds, contributing to their diverse range of colors and functions.
Uses
Used in Pharmaceutical Industry:
Farnesylacetone is used as a precursor in the synthesis of various pharmaceutical compounds, particularly those related to the production of carotenoids. Its involvement in the biosynthesis process makes it a valuable component in the development of drugs and supplements that target specific health benefits associated with carotenoids.
Used in Cosmetic Industry:
In the cosmetic industry, farnesylacetone is utilized as a key ingredient in the formulation of products that aim to enhance skin health and appearance. Its role in carotenoid synthesis contributes to the development of cosmetics that promote skin protection, hydration, and rejuvenation.
Used in Nutraceutical Industry:
Farnesylacetone is employed as a vital component in the production of nutraceuticals, which are substances that provide additional health benefits beyond basic nutrition. Its presence in the synthesis of carotenoids allows for the creation of supplements and functional foods that support overall health and well-being.
Used in Agricultural Industry:
In agriculture, farnesylacetone plays a significant role in the enhancement of crop quality and yield. Its involvement in carotenoid biosynthesis can lead to the development of plant varieties with improved nutritional content, color, and resistance to various environmental stressors.
Overall, farnesylacetone's applications span across multiple industries, primarily due to its essential function in the biosynthesis of carotenoids. Its versatility and importance in various fields highlight its potential for further research and development in the future.
Preparation
By treating farnesyl bromide with sodium acetate, followed by treating with methanolic KOH.
Check Digit Verification of cas no
The CAS Registry Mumber 762-29-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 762-29:
(5*7)+(4*6)+(3*2)+(2*2)+(1*9)=78
78 % 10 = 8
So 762-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H30O/c1-15(2)9-6-10-16(3)11-7-12-17(4)13-8-14-18(5)19/h9,11,13H,6-8,10,12,14H2,1-5H3/b16-11+,17-13-
762-29-8Relevant articles and documents
Method for synthesizing farnesyl acetone
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Paragraph 0006; 0012-0017, (2021/11/21)
The invention discloses a method for synthesizing farnesyl acetone. The method comprises the following steps of: mixing nerolidol and aluminum oxide, heating, dropwise adding methyl acetoacetate, carrying out heat preservation reaction after dropwise adding, evaporating generated methanol in the reaction process, and collecting generated carbon dioxide gas; and after finishing the reaction, filtering and separating aluminum oxide, and carrying out reduced pressure distillation on filtrate to collect the product farnesyl acetone. According to the method, the reaction yield is high, a catalyst can be separated through filtration and can be reused, washing of the reaction materials is avoided; waste water and waste containing metal ions are not generated, so that pollution to the environment is avoided; and generated by-products including methanol and carbon dioxide can be recycled.
MANUFACTURE OF GAMMA-DELTA-UNSATURATED KETONES
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Page/Page column 7, (2010/05/13)
A process for the manufacture of gamma-delta-unsaturated ketones of formula (R1)(R2)C = CH - CH2 - CH2 - CO - R3 (I), wherein R1 is methyl or ethyl; R2 is a saturated or unsaturated linear or cyclic hydrocarbon residue and R3 is methyl or ethyl, by reacting a tertiary vinyl carbinol of formula (R1)(R2)C(OH) - CH = CH2 (II) with an isopropenyl methyl or ethyl ether of formula H3C-C(OR3) = CH2 (III) in the presence of an ammonium salt as catalyst.
THE CARROLL REARRANGEMENT ON THE SURFACE OF CHROMATOGRAPHIC ABSORBENTS
Smit, V. A.,Pogrebnoi, S. I.,Kal'yan, Yu. B.,Krimer, M. Z.
, p. 888 (2007/10/02)
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