31825-29-3

Basic information

• Product Name: 3-ISOPROPYL-4-METHOXYBENZOALDEHYDE
• Synonyms: 3-ISOPROPYL-4-METHOXYBENZOALDEHYDE;Benzaldehyde,4-Methoxy-3-(1-Methylethyl)-;4-methoxy-3-propan-2-ylbenzaldehyde
• CAS NO: 31825-29-3
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.23
• Mol File: 31825-29-3.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 284.736°C at 760 mmHg
• Flash Point: 121.707°C
• Appearance: /
• Density: 1.017g/cm³
• Vapor Pressure: 0.003mmHg at 25°C
• Refractive Index: 1.527
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 3-ISOPROPYL-4-METHOXYBENZOALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ISOPROPYL-4-METHOXYBENZOALDEHYDE(31825-29-3)
• EPA Substance Registry System: 3-ISOPROPYL-4-METHOXYBENZOALDEHYDE(31825-29-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 31825-29-3(Hazardous Substances Data)

Usage

General Description

3-ISOPROPYL-4-METHOXYBENZOALDEHYDE is a chemical compound that is commonly used in the fragrance and flavor industry. It is a colorless to pale yellow liquid with a sweet, floral, and fruity odor. 3-ISOPROPYL-4-METHOXYBENZOALDEHYDE is primarily used as a fragrance ingredient in various personal care products, including perfumes, soaps, and lotions. It is also used as a flavoring agent in food and beverages. Additionally, 3-ISOPROPYL-4-METHOXYBENZOALDEHYDE has been studied for its potential pharmaceutical applications, including its antimicrobial and antioxidant properties. Its chemical structure and properties make it a versatile and valuable ingredient in a wide range of industries.

InChI:InChI=1/C11H14O2/c1-8(2)10-6-9(7-12)4-5-11(10)13-3/h4-8H,1-3H3

Upstream product

• 4885-02-3 Dichloromethyl methyl ether 
• 2944-47-0 o-isopropylanisole 
• 39863-70-2 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol 
• 76-05-1 trifluoroacetic acid 
• 80041-89-0 isopropylboronic acid 
• 157790-73-3 4-methoxy-3-trifluoromethanesulfonyloxybenzaldehyde 
• 621-59-0 isovanillin 
• 2591-86-8 N-Formylpiperidine 
• 24591-33-1 4-bromo-2-isopropylanisole 
• 88-69-7 2-(1-methylethyl)phenol 
• 68-12-2 N,N-dimethyl-formamide 
• 134435-48-6 3-(1-methylethenyl)-4-methoxyphenylethyl acetate 
• 134435-50-0 (3-Isopropyl-4-methoxy-phenyl)-acetaldehyde 
• 702-23-8 2-(4-Methoxyphenyl)ethanol 

Downstream Products

• 936363-23-4 β-dibromo-3-isopropyl-4-methoxystyrene 
• 31859-25-3 4-Methoxy-3-isopropylphenylacetonitrile 
• 64929-62-0 3-isopropyl-4-methoxybenzyl bromide 
• 134435-51-1 2-Geranyl-2-(3-isopropyl-4-methoxyphenyl)acetonitrile 
• 61494-73-3 3,7-Diketo-12-hydroxyabieta-8,11,13-triene 
• 134435-54-4 7-Keto-3-phenylthio-12-methoxyabieta-2,8,11,13-tetraene 
• 134435-53-3 7-Oxo-3-phenylthio-12-methoxyabieta-8,11,13-triene 
• 134435-55-5 7-Keto-3-phenylsulfinyl-12-methoxyabieta-8,11,13-triene 
• 134435-52-2 7-Cyano-3-phenylthio-12-methoxyabieta-8,11,13-triene 
• 134435-51-1 (E)-2-(3-Isopropyl-4-methoxy-phenyl)-5,9-dimethyl-deca-4,8-dienenitrile 
• 61494-73-3 12-hydroxy-abieta-8,11,13-trien-3,7-dione 
• 134435-54-4 7-Isopropyl-6-methoxy-1,1,4a-trimethyl-2-phenylsulfanyl-4,4a,10,10a-tetrahydro-1H-phenanthren-9-one 
• 134435-53-3 7-Isopropyl-6-methoxy-1,1,4a-trimethyl-2-phenylsulfanyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 
• 134435-55-5 2-Benzenesulfinyl-7-isopropyl-6-methoxy-1,1,4a-trimethyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 

Relevant articles and documents

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A sulfenium-ion-initiated, catalytic, enantioselective polyene cyclization is described. Homogeranylarenes and ortho-geranylphenols undergo polycyclization in good yield, diastereoselectivity, and enantioselectivity. The stereodetermining step is the generation of an enantiomerically enriched thiiranium ion from a terminal alkene and a sulfenylating agent in the presence of a chiral Lewis basic catalyst. The use of hexafluoroisopropyl alcohol as the solvent is crucial to obtain good yields. The thioether moiety resulting from the reaction can be subsequently transformed into diverse oxygen and carbon functionality postcyclization. The utility of this method is demonstrated by the enantioselective syntheses of (+)-ferruginol and (+)-hinokiol.

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