38770-70-6

Basic information

• Product Name: Phenol, 3-methyl-4-(1-methylethyl)-, acetate
• CAS NO: 38770-70-6
• Molecular Formula: C12H16O2
• Molecular Weight: 192.258
• Mol File: 38770-70-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phenol, 3-methyl-4-(1-methylethyl)-, acetate(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-methyl-4-(1-methylethyl)-, acetate(38770-70-6)
• EPA Substance Registry System: Phenol, 3-methyl-4-(1-methylethyl)-, acetate(38770-70-6)

Safety Data

• Hazardous Substances Data: 38770-70-6(Hazardous Substances Data)

Upstream product

• 18309-32-5 Verbenone 
• 108-24-7 acetic anhydride 
• 557-34-6 zinc diacetate 
• 3228-02-2 3-Methyl-4-isopropylphenol 
• 75-36-5 acetyl chloride 

Downstream Products

• 109694-22-6 2-(6-hydroxy-3-isopropyl-2-methyl-phenyl)-quinoline-4-carboxylic acid 
• 102883-93-2 2-[2]quinolyl-4-isopropyl-3-methyl-phenol 
• 52774-08-0 1-<2-hydroxy-4-methyl-5-(1-methylethyl)phenyl>-1-ethanone 
• 105337-35-7 1-<6-hydroxy-2-methyl-3-(1-methylethyl)phenyl>-ethanone 

Relevant articles and documents

INSECTICIDAL COMPOSITION

PROBLEM TO BE SOLVED: To provide a composition that can exhibit effective insecticidal action on insect pests. SOLUTION: An insecticidal composition comprises, e.g., a compound represented by general formula (1) in the figure. [R1 is a C1-10 alkyl group or the like, where the alkyl group and the like may be substituted with a halogen atom or the like; R2 is a hydrogen atom or the like, or R2 may bind a methoxy group binding a carbon atom adjacent to a carbon atom which R2 binds, to form a -O-CH2-O- group.] SELECTED DRAWING: None COPYRIGHT: (C)2021,JPO&INPIT

Reactions of some terpenes and their derivatives with acylating agents in the presence of aluminosilicate catalysts

Reactions of camphene, α-fenchene, limonene, caryophyllene, α- and β-pinenes, verbenol, walterol, and verbenone with acylating agents in the presence of clay K-10 and wide-porous β-zeolite were studied. Presumable schemes and rules of the occurring proces

Lewis Acids Catalysed Fries Rearrangement of Isopropylcresol Esters

In the course of the Fries rearrangement, aluminium chloride frequently induces migration or elimination of alkyl groups.The results obtained with titanium tetrachloride for the synthesis of vicinal o-hydroxyketones are compared with those obtained with aluminium chloride for some aliphatic and aromatic esters of isopropylcresols.In order to understand the migration and elimination processes occurring, the stabilities of the o-hydroxyketones are studied in the presence of aluminium chloride at different temperatures.Furthermore, all-vicinal o-hydroxyketones were prepared by the Fries rearrangement of 6-tert-butyl-p-thymol with titanium tetrachloride.