5779-95-3 Usage
Description
3,5-Dimethylbenzaldehyde is an organic compound with the chemical formula C9H10O. It is a clear colorless to yellow liquid and is known for its distinct aromatic smell. 3,5-Dimethylbenzaldehyde is an aromatic aldehyde derived from benzene, with two methyl groups attached at the 3rd and 5th positions. It is widely used in various industries due to its unique chemical properties and versatile applications.
Uses
Used in Chemical Synthesis:
3,5-Dimethylbenzaldehyde is used as a key intermediate in the production of various chemicals. For instance, it is used to produce 2,3-bis-(3,5-dimethyl-phenyl)-succinonitrile by heating along with the reagent NaCN and solvent H2O, methanol. This synthesized compound has potential applications in the chemical and pharmaceutical industries.
Used in Flavor and Fragrance Industry:
3,5-Dimethylbenzaldehyde is used as a flavoring agent and a fragrance ingredient in the food, beverage, and cosmetic industries. Its distinct aromatic smell makes it a valuable component in creating various scents and flavors for different products.
Used in Pharmaceutical Industry:
Due to its chemical properties, 3,5-Dimethylbenzaldehyde can be utilized in the synthesis of pharmaceutical compounds. It can serve as a building block for developing new drugs or improving the efficacy of existing ones.
Used in Dye and Pigment Industry:
3,5-Dimethylbenzaldehyde's chemical structure also makes it suitable for use in the dye and pigment industry. It can be employed in the production of various dyes and pigments, contributing to the coloration of textiles, plastics, and other materials.
Check Digit Verification of cas no
The CAS Registry Mumber 5779-95-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5779-95:
(6*5)+(5*7)+(4*7)+(3*9)+(2*9)+(1*5)=143
143 % 10 = 3
So 5779-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O/c1-7-3-8(2)5-9(4-7)6-10/h3-6H,1-2H3
5779-95-3Relevant articles and documents
An expeditious and efficient method for the oxidation of benzyl alcohols by homogeneous electrolysis
Jagatheesan, Rathinavel,Shanmugavelan, Poovan,Sambathkumar, Subramaniyan,Ramesh, Pugalenthi
supporting information, p. 3013 - 3022 (2021/08/12)
A greener and inexpensive electrochemical method has been developed for the oxidation of benzyl alcohols by homogeneous electrolysis. The electrochemical reaction was carried out in an undivided cell equipped with carbon and stainless steel electrodes at room temperature. The homogeneous solution made up of acetonitrile/water containing substrate and ammonium bromide with a catalytic amount of H2SO4 as supporting electrolyte. The reaction condition was optimized with various electrochemical experimental parameters and evaluated with various substituted benzyl alcohols to result in excellent yield of aldehydes (>83%).
Visible-Spectrum Solar-Light-Mediated Benzylic C-H Oxygenation Using 9,10-Dibromoanthracene As an Initiator
Santra, Sourav K.,Szpilman, Alex M.
, p. 1164 - 1171 (2020/12/23)
We report a visible-light-mediated benzylic C-H oxygenation reaction. The reaction is initiated by solar light or the blue LED activation of 9,10-dibromoanthracene in a reaction with oxygen and takes place at ambient temperature and air pressure. Secondary benzylic positions are oxygenated to ketones, while tertiary benzylic carbons are oxygenated to give hydroperoxides. Notably, cumene hydroperoxide is produced in a higher yield and at milder conditions than the currently employed industrial conditions.
LIGHT INDUCED CATALYTIC C-H OXYGENATION OF ALKANES
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Paragraph 00219, (2021/04/02)
A method of oxygenating a benzylic C-H bond is provided. The method comprises light induced activation of an initiator and subsequent reaction with oxygen, resulting in the formation of free radicals. Subsequently, free radicals catalyze the reaction of the benzylic C-H bond with oxygen, thereby forming an oxygenated compound.