3125-36-8

Basic information

• Product Name: 1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol
• Synonyms: 1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol;6-Methoxy-1-vinyl-1,2,3,4-tetrahydronaphthalen-1-ol
• CAS NO: 3125-36-8
• Molecular Formula: C₁₃H₁₆O₂
• Molecular Weight: 204.26
• Mol File: 3125-36-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol(3125-36-8)
• EPA Substance Registry System: 1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol(3125-36-8)

Safety Data

• Hazardous Substances Data: 3125-36-8(Hazardous Substances Data)

Usage

General Description

1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol is a chemical compound with a long and complex name, commonly known as 6-Methoxy-1-tetralol or PMNT. 1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol is a naphthalenol derivative, which is a type of fragrance ingredient commonly used in perfumes and cosmetics for its pleasant and warm scent. It is also used as a flavoring agent in food products. PMNT is a clear, colorless to pale yellow liquid with a floral and sweet odor. It is primarily used in the fragrance industry to add a woody, floral, and slightly fruity note to perfumes and colognes. Additionally, it is used in the production of soaps, detergents, and other cosmetic products.

Upstream product

• 1826-67-1 vinyl magnesium bromide 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 

Downstream Products

• 966-46-1 13β-Methyl-3-methoxygona-1,3,5(10),9-tetraen-17-on 
• 17908-45-1 (8S,13S,14S)-14-hydroxy-3-methoxy-13-methyl-6,7,8,12,13,14,15,16-octahydro-17H-cyclopenta[a]phenanthren-17-one 
• 5067-45-8 2-<2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ylidene)ethyl>-2-methylcyclohexane-1,3-dione 
• 850-92-0 2-[2-(3,4-dihydro-6-methoxy-1(2H)-naphthalenylidene)ethyl]-2-ethyl-1,3-cyclopentanedione 
• 26584-90-7 7-Methoxy-3'-methyl-1,2-cyclopentano-phenanthren 
• 827008-26-4 2-[2-(6-methoxy-3,4-dihydro-2H-naphthalen-1-ylidene)-ethyl]-2-methyl-3-vinyl-cyclohexanone 
• 827008-20-8 2-[2-(6-methoxy-3,4-dihydro-2H-naphthalen-1-ylidene)-ethyl]-2-methyl-cyclohexanone 
• 899-79-6 2-[2-(3,4-dihydro-6-methoxy-1(2H)-naphthalenylidene)ethyl]-2-methyl-1,3-cyclopentanedione 
• 2811-50-9 7-methoxy-4-vinyl-1,2-dihydronaphthalene 

Relevant articles and documents

Chemical consequences of fluorine substitution. Part 4. Diels-Alder reactions of fluorinated p-benzoquinones with Dane's diene. Synthesis of fluorinated D-homosteroids

Four fluorinated p-benzoquinones (2) have been reacted with Dane's diene (1) in Diels-Alder reactions and the formed fluorinated D-homosteroids were characterized. The number of products, their stereochemistry and stability depends on the fluorine substitution pattern of the corresponding fluorinated p-benzoquinones. If the p-benzoquinone (2) contains an unfluorinated double bond, this bond reacts faster with diene 1 yielding endo-products selectively. In contrast, [4+2]cycloadditions with 2,6-difluoro (2c) and 2,3,5,6-tetrafluorobenzoquinone (2d) gave the products with exo-orientation of the carbonyl part preferably.