24894-78-8

Basic information

• Product Name: 1-Naphthalenol,6-methyl-(9CI)
• Synonyms: 1-Naphthalenol,6-methyl-(9CI);6-Methyl-1-naphthol;1-Hydrocy-6-methylnaphthalene;6-METHYLNAPHTHALEN-1-OL
• CAS NO: 24894-78-8
• Molecular Formula: C₁₁H₁₀O
• Molecular Weight: 158.199
• Product Categories: NAPHTALENE
• Mol File: 24894-78-8.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Naphthalenol,6-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenol,6-methyl-(9CI)(24894-78-8)
• EPA Substance Registry System: 1-Naphthalenol,6-methyl-(9CI)(24894-78-8)

Safety Data

• Hazardous Substances Data: 24894-78-8(Hazardous Substances Data)

Usage

Description

1-Naphthalenol,6-methyl-(9CI), also known as 6-methylnaphth-1-ol, is a chemical compound belonging to the naphthalenol family. With the molecular formula C11H10O, this white to off-white solid exhibits a strong odor. It is recognized for its use as a synthetic intermediate in the production of various organic compounds and contributes to the manufacturing of fragrances and flavors. Due to its irritant properties, it requires careful handling to prevent skin and eye irritation, and its potential environmental impact on aquatic organisms necessitates responsible handling and disposal.

Uses

Used in Organic Synthesis:
1-Naphthalenol,6-methyl-(9CI) is used as a synthetic intermediate for the production of various organic compounds. Its unique chemical structure allows it to be a key component in the synthesis of a range of chemical products, contributing to the versatility and functionality of the final products.
Used in Fragrance and Flavor Industry:
In the fragrance and flavor industry, 1-Naphthalenol,6-methyl-(9CI) is utilized for its distinctive aromatic properties. It serves as a valuable ingredient in creating complex and appealing scents and tastes, enhancing the sensory experience of consumer products.
Used in Research and Development:
1-Naphthalenol,6-methyl-(9CI) also finds application in research and development settings, where its chemical properties are studied and explored for potential new uses and applications. This includes investigations into its reactivity, stability, and interactions with other compounds, which can lead to innovative discoveries and advancements in various fields.

Upstream product

• 51015-29-3 6-methyl-3,4-dihydronaphthalen-1(2H)-one 
• 54714-43-1 2-bromo-6-methyltetralone 
• 91-66-7 N,N-diethylaniline 
• 19061-31-5 1,4-dihydro-1,4-epoxy-6-methylnaphthalene 
• 88-14-2 2-furanoic acid 
• 90500-13-3 5-methyl-2-iodosylbenzoic acid 
• 72839-13-5 1-(2,6-dimethylphenyl)-2-propyn-1-one 
• 91270-68-7 6-bromo-α-naphthol 
• 544-97-8 dimethyl zinc(II) 
• 66361-67-9 6-bromo-3,4-dihydro-2H-naphthalen-1-one 
• 3470-53-9 6-amino-1-tetralone 
• 24894-75-5 1-Methoxy-6-methyl-naphthalin-3-carbonsaeure-methylester 
• 24894-76-6 1-Methoxy-6-methyl-naphthalin-3-carbonsaeure 
• 52548-14-8 2-iodoyl-5-methylbenzoic acid 

Relevant articles and documents

ARYNIC SPECIES II; TOSYL AND TRIAZENE AS LEAVING GROUP IN THE GENERATION OF ARYNES FROM POLYMER-BOUND REAGENTS

o-Benzyne and its 4-methyl, 4-chloro and 4-bromo-derivatives were generated in the thermal decomposition of two new kinds of polymer-bound precursors: 1(2-carboxyaryl)triazenes and 2-carboxyaryl-sulphonates.New kinds of trapping polymers for these elusive

Picomolar inhibitors of HIV-1 reverse transcriptase: Design and crystallography of naphthyl phenyl ethers

Catechol diethers that incorporate a 6-cyano-1-naphthyl substituent have been explored as non-nucleoside inhibitors of HIV-1 reverse transcriptase (NNRTIs). Promising compounds are reported that show midpicomolar activity against the wild-type virus and sub-20 nM activity against viral variants bearing Tyr181Cys and Lys103Asn mutations in HIV-RT. An X-ray crystal structure at 2.49 ? resolution is also reported for the key compound 6e with HIV-RT.

The Gas-Flow Thermolysis of 1-Isobutenyl Alkynyl and 2-Methylphenyl Alkynyl Ketones. Synthesis of Methylenomycin B

The gas-flow thermolysis of 1-isobutenyl alkynyl or 2-methyphenyl alkynyl ketones were found to lead to phenols and cyclopentenones or to naphthols and indanones, respectively.These conversions involve two cyclization processes so far unknown with α-alkynones; they are interpreted as intramolecular additions of an allylic or a benzylic C,H bond to a triple bond which may occur in two directions.In addition, the cyclopentenones formed by the α-alkynone cyclization, a known carbene process yielding 5-rings, were also found.The available evidence ruled out a carbene process yielding 6-rings.The addition process yielding 5-rings was applied to a short (but low yield) synthesis of methylenomycin B.