5340-85-2

Usage

Uses

Used in Fragrance Industry:
2,4-DIMETHYL-4-PHENYLPENTAN-2-OL is used as a fragrance ingredient for its slightly floral or sweet odor, contributing to the scent profiles of perfumes and other scented products.
Used in Chemical Production:
2,4-DIMETHYL-4-PHENYLPENTAN-2-OL is used in the production of various chemical products, such as pharmaceuticals and pesticides, due to its versatile chemical properties.
Used in Antimicrobial Applications:
2,4-DIMETHYL-4-PHENYLPENTAN-2-OL is used as an antimicrobial agent, exhibiting properties that can help inhibit the growth of certain microorganisms, making it potentially useful in a range of applications where microbial control is necessary.
Used in Antioxidant Applications:
2,4-DIMETHYL-4-PHENYLPENTAN-2-OL is used as an antioxidant, which can help prevent or slow down the oxidation of other substances. This property can be beneficial in various industries where oxidation might lead to degradation or spoilage.

InChI:InChI=1/C13H20O/c1-12(2,10-13(3,4)14)11-8-6-5-7-9-11/h5-9,14H,10H2,1-4H3

Upstream product

• 917-64-6 methyl magnesium iodide 
• 7403-42-1 4-Methyl-4-phenyl-2-pentanone 
• 25080-84-6 3-Methyl-3-phenylbutansaeure-methylester 
• 35293-35-7 2-methyl-2-phenyl-1-propylmagnesium chloride 
• 676-58-4 methylmagnesium chloride 
• 515-40-2 neophyl chloride 
• 67-64-1 acetone 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 71-43-2 benzene 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 7403-42-1 4-Methyl-4-phenyl-2-pentanone 
• 4406-52-4 (1,1,3-trimethylbutyl)benzene 
• 61455-14-9 N-(1,1,3-trimethyl-3-phenylbutyl)formamide 
• 132595-48-3 2,4-dimethyl-4-phenyl-1-pentene 
• 92104-77-3 2,4-dimethyl-4-phenyl-2-pentene 
• 826-55-1 2-methyl-2-phenylpropionic acid 
• 98-86-2 acetophenone 
• 35322-23-7 1,4-Diphenyl-2,2,4-trimethylpentan 
• 61455-11-6 Bis-(1,1,3-trimethyl-3-phenyl-butyl)-diazene 
• 76613-28-0 N,N'-bis(1,1,3-trimethyl-3-phenylbutyl)thiadiaziridine 1,1-dioxide 
• 61455-16-1 N,N'-bis(1,1,3-trimethyl-3-phenylbutyl)sulfamide 
• 61455-15-0 1,1,3-trimethyl-3-phenylbutylamine 

Relevant academic research and scientific papers

Disubstituted chalcone oximes as selective agonists of RAR retinoid receptors

Compounds of the formula where the variables are as defined in the specification, are useful for preventing or treating emphysema and related pulmonary conditions of mammals and other diseases and conditions which are responsive to RARγ agonist retinoids, such as skin related diseases, including but not limited to acne and psoriasis.

THE EFFECT OF THE POSITION OF THE DOUBLE BOND ON THE MECHANISM OF INTRAMOLECULAR CYCLOALKYLATION OF 2,4-DIMETHYL-4-PHENYLPENTENES IN SULFURIC ACID

Hydrogen exchange during the intramolecular cycloalkylation of 2,4-dimethyl-4-phenyylpentenes in 85percent sulfuric acid was studied by NMR and mass spectrometry. It was shown on the basis of the distribution of deuterium in 1,1,3,3-tetramethylindane that during cyclization of the endo-chain olefin the obtained γ-phenylalkyl cation undergoes partial deprotonation with the formation of an isomeric olefin whereas protonation of the terminal double bond is accompanied by rapid alkylation of the aromatic ring.