86604-05-9

Basic information

• Product Name: 4-ISOPROPYLCINNAMALDEHYDE
• Synonyms: 4-ISOPROPYLCINNAMALDEHYDE
• CAS NO: 86604-05-9
• Molecular Formula: C₁₂H₁₄O
• Molecular Weight: 174.24
• Mol File: 86604-05-9.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-ISOPROPYLCINNAMALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ISOPROPYLCINNAMALDEHYDE(86604-05-9)
• EPA Substance Registry System: 4-ISOPROPYLCINNAMALDEHYDE(86604-05-9)

Safety Data

• Hazardous Substances Data: 86604-05-9(Hazardous Substances Data)

Usage

General Description

4-Isopropylcinnamaldehyde is a chemical compound that is commonly used as a flavoring agent in food and beverages, as well as a fragrance in perfumes and cosmetics. It is a pale yellow liquid with a floral and powdery odor, and is derived from the cinnamaldehyde molecule. 4-Isopropylcinnamaldehyde has been found to exhibit anti-inflammatory, antioxidant, and antimicrobial properties, making it useful for various applications in the pharmaceutical and personal care industries. Additionally, it is used in the synthesis of other compounds, and has potential use in the development of new drugs and treatments. Despite its potential benefits, it is important to handle 4-isopropylcinnamaldehyde with caution due to its potential irritant and sensitizing effects.

Upstream product

• 876473-87-9 3-chloro-1-(4-isopropyl-phenyl)-propene 
• 64-17-5 ethanol 
• 100-97-0 hexamethylenetetramine 
• 27546-49-2 4-isopropyl-1-cyclopropylbenzene 
• 29805-21-8 1-(4-isopropylphenyl)-2-propyn-1-ol 
• 86657-74-1 1-Isopropyl-4-(1,3,3-triethoxy-propyl)-benzene 
• 274907-08-3 (E)-3-(4-isopropylphenyl)-2-propen-1-ol 
• 128408-02-6 ethyl (E)-3-(4-isopropylphenyl)-2-propenoate 
• 67785-72-2 dimethoxycymene 
• 98-82-8 Isopropylbenzene 
• 123-38-6 propionaldehyde 
• 122-03-2 (4-isopropylbenzaldehyde) 
• 86657-68-3 1-(4-Isopropyl-phenyl)-2-(4,4,6-trimethyl-5,6-dihydro-4H-[1,3]oxazin-2-yl)-ethanol 

Downstream Products

• 7402-35-9 4-isopropyl-cinnamaldehyde-(4-isobutyl thiosemicarbazone) 
• 351536-36-2 (E)-1,1,1-Trichloro-4-(4-isopropyl-phenyl)-but-3-en-2-ol 
• 351536-17-9 2-tert-butyldimethylsilyloxy-1,1,1-trichloro-4-(4-isopropylphenyl)-3-butene 
• 1208865-02-4 (S)-2-(3-oxo-1-(4-isopropylphenyl)propyl)malonic acid dibenzyl ester 
• 1208865-03-5 (R)-2-(3-oxo-1-(4-isopropylphenyl)propyl)malonic acid dibenzyl ester 

Relevant articles and documents

Amino acid derivative, feed composition and application thereof

The invention provides an amino acid derivative, a feed composition and application thereof, and belongs to the technical field of animal feed additives. The amino acid derivative is a compound with astructure shown as a formula (I), and a stereoisomer, a tautomer, a solvate, a metabolite, a feed acceptable salt or a prodrug thereof. In formula (I) shown in the specification, Z is a C1-C3 alkylene group. X is an indole ring group with a structure shown as a formula (II). The formula (II) is shown in the specification, wherein Y is phenyl with the structure shown in the formula (III) shown inthe specification. The amino acid derivative is used as an animal feed additive, and can promote the growth of animals and improve the feed conversion.

Iron(III)/O2-Mediated Regioselective Oxidative Cleavage of 1-Arylbutadienes to Cinnamaldehydes

A simple, efficient, and environmentally benevolent regioselective oxidative cleavage of 1-arylbutadienes to cinnamaldehydes mediated by iron(III) sulfate/O2 has been developed. The reaction offered good yields and excellent regioselectivity and showed good functional group tolerance (31 examples). The method is important, as few reports with limited substrate scope are available for such excellent oxidative cleavage of conjugated dienes.

Kinetic resolution of acyclic secondary allylic silyl ethers catalyzed by chiral ketones

Kinetic resolution of acyclic secondary allylic silyl ethers by chiral dioxiranes generated in situ from chiral ketones (R)-1 and (R)-2 and Oxone was investigated. An efficient and catalytic method has been developed for kinetic resolution of those substrates with a CCl3, tert-butyl, or CF3 group at the α-position. In particular, high selectivities (S up to 100) were observed for kinetic resolutions of racemic α-trichloromethyl allylic silyl ethers 7 and 9-15 catalyzed by ketones (R)-2. Both the recovered substrates and the resulting epoxides were obtained in high enantiomeric excess. On the basis of steric and electrostatic interactions between the chiral dioxiranes and the racemic substrates, a model was proposed to rationalize the enantioselectivities and diastereoselectivities in the chiral ketone-catalyzed kinetic resolution process.