55846-68-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, 1,3-Octanedione, 1-phenylhas 12 carbon (C) atoms, 18 hydrogen (H) atoms, and 2 oxygen (O) atoms.
Explanation
A diketone is an organic compound that contains two carbonyl groups (C=O). In 1,3-Octanedione, 1-phenyl-, these carbonyl groups are located at the 1 and 3 positions of the octane chain.
Explanation
The phenyl group (C6H5) is attached to the 1 position of the octane chain, making it a 1-phenyl-substituted diketone.
Explanation
1,3-Octanedione, 1-phenylcan be found naturally in some fruits and vegetables, contributing to their unique flavors and aromas.
Explanation
Due to its sweet, fruity odor, 1,3-Octanedione, 1-phenylis commonly used as a flavoring agent in the food and beverage industry.
Explanation
The compound is also used in the production of various fragrances and perfumes, taking advantage of its pleasant odor.
Explanation
1,3-Octanedione, 1-phenylis considered safe for consumption when used in small amounts, as it is a naturally occurring compound in some fruits and vegetables.
Explanation
Although safe at low levels, high doses of 1,3-Octanedione, 1-phenylcan be toxic, and its use should be carefully regulated.
Explanation
The compound may have potential uses in the pharmaceutical and cosmetic industries, possibly due to its unique properties or effects.
Explanation
1,3-Octanedione, 1-phenylis known for its sweet, fruity odor, which makes it a desirable compound for use in the flavoring and fragrance industries.
Type of Compound
Diketone
Phenyl Group Attachment
1 position
Natural Occurrence
Found in certain fruits and vegetables
Application
Flavoring agent
Usage in Manufacturing
Fragrances and perfumes
Safety
Safe for consumption at low levels
Toxicity
High doses can be toxic
Potential Applications
Pharmaceutical and cosmetic industries
Odor
Sweet, fruity
Check Digit Verification of cas no
The CAS Registry Mumber 55846-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,4 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55846-68:
(7*5)+(6*5)+(5*8)+(4*4)+(3*6)+(2*6)+(1*8)=159
159 % 10 = 9
So 55846-68-9 is a valid CAS Registry Number.
55846-68-9Relevant academic research and scientific papers
Palladium-Catalyzed Oxidative Alkoxylation of α-Alkenyl β-Diketones to Form Functionalized Furans
Han, Xiaoqing,Widenhoefer, Ross A.
, p. 1738 - 1740 (2007/10/03)
Treatment of 4-allyl-2,6-dimethyl-3,5-heptanedione with a catalytic amount of PdCl2(CH3CN)2 (5 mol %) and a stoichiometric amount of CuCl2 (2.2 equiv) in dioxane at 60 °C for 12 h formed 3-isobutyryl-2-isopropyl-5-methylfuran in 77% isolated yield. A number of α-alkenyl β-dike-tones underwent oxidative alkoxylation under these conditions to form 2,3,5-trisubsituted furans in moderate to good yield.
A novel synthesis of 1,3-diketones by reaction of an α-bromoketone with acyl chlorides promoted by gallium triiodide
Chen, Rener,Wu, Huayue,Zhang, Yongmin
, p. 666 - 667 (2007/10/03)
Promoted by gallium triiodide, an α-bromoketone, bromomethyl phenyl ketone, is treated with acyl chlorides to synthesize 1,3-diketones in good yields under mild and neutral conditions.
β-Diketone synthesis by reaction of α-haloketones with acid chlorides or acid anhydrides promoted by samarium triiodide
Ying, TaoKai,Bao, Weiliang,Zhang, Yongmin
, p. 2905 - 2909 (2007/10/03)
Promoted by SmI3, α-haloketones were reacted with acid chlorides or acid anhydrides and β-diketones were synthesized via intermediate samarium enolates.
An alternative route to 1,3-diketones promoted by samarium diiodide
Ying, Taokai,Bao, Weiliang,Zhang, Yongmin,Xu, Weinming
, p. 3885 - 3886 (2007/10/03)
Sml2 promoted condensation of α-haloketones with carboxylic acid chlorides or anhydrides leads to 1,3-diketones.
