13577-40-7

Basic information

• Product Name: 1-(5,6,7,8-TETRAHYDRO-NAPHTHALEN-1-YL)-ETHANONE
• Synonyms: 1-(5,6,7,8-TETRAHYDRO-NAPHTHALEN-1-YL)-ETHANONE;1-(1,2,3,4-tetrahydronaphthalen-5-yl)ethanone
• CAS NO: 13577-40-7
• Molecular Formula: C₁₂H₁₄O
• Molecular Weight: 174.23896
• Mol File: 13577-40-7.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 309.1°C at 760 mmHg
• Flash Point: 132°C
• Appearance: /
• Density: 1.038g/cm³
• Vapor Pressure: 0.000653mmHg at 25°C
• Refractive Index: 1.545
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-(5,6,7,8-TETRAHYDRO-NAPHTHALEN-1-YL)-ETHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(5,6,7,8-TETRAHYDRO-NAPHTHALEN-1-YL)-ETHANONE(13577-40-7)
• EPA Substance Registry System: 1-(5,6,7,8-TETRAHYDRO-NAPHTHALEN-1-YL)-ETHANONE(13577-40-7)

Safety Data

• Hazardous Substances Data: 13577-40-7(Hazardous Substances Data)

Usage

General Description

1-(5,6,7,8-Tetrahydro-naphthalen-1-yl)-ethanone is a chemical compound with the molecular formula C14H16O. It is a ketone derivative of tetrahydronaphthalene, and is also known as 1-tetralone. It is commonly used in the synthesis of pharmaceuticals, agrochemicals, and fragrances. As a fragrance ingredient, it has a floral, citrus-like odor. It also has industrial applications as a solvent and intermediate in the production of organic compounds. Additionally, it has been investigated for its potential biological activities, including as an antifungal and antibacterial agent.

InChI:InChI=1/C12H14O/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h4,6,8H,2-3,5,7H2,1H3

Upstream product

• 941-98-0 1'-naphthacetophenone 
• 101533-70-4 trifluoro-methanesulfonic acid 5,6,7,8-tetrahydro-naphthalen-1-yl ester 
• 529-35-1 5,6,7,8-Tetrahydronaphthalen-1-ol 
• 28315-93-7 5-Hydroxy-1-tetralone 
• 12154-63-1 tricarbonyl{(4a,5,6,7,8,8a-η)-1,2,3,4-tetrahydronaphthalene}chromium(0) 
• 27969-97-7 2-lithio-2-methyl-1,3-dithiane 
• 86-55-5 1-naphthalenecarboxylic acid 
• 119-64-2 tetralin 
• 69849-04-3 2-(1-ethoxyethoxy)-2-lithiopropanenitrile 
• 108-24-7 acetic anhydride 
• 110808-69-0 5,6,7,8-tetrahydronaphthylene-1-carboxylic acid chloride 
• 75-16-1 methylmagnesium bromide 
• 4242-18-6 5,6,7,8-tetrahydro-1-naphthalenecarboxylic acid 
• 917-54-4 methyllithium 

Downstream Products

• 110424-25-4 3-phenyl-2,3,6,7,8,9-hexahydro-1H-cyclopenta[a]naphthalene 
• 110937-79-6 3-phenyl-2,3,6,7,8,9-hexahydro-cyclopenta[a]naphthalen-1-one 
• 71432-09-2 1-Phenyl-2-(5,6,7,8-tetrahydro-naphthalen-1-yl)-propan-2-ol 
• 941-98-0 1'-naphthacetophenone 
• 1127-76-0 1-ethylnapthelene 

Relevant articles and documents

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TETRAZOLINONE COMPOUND AND USE THEREOF

The compound represented by formula (1): wherein R4 and R5 each represents a hydrogen atom, a halogen atom, or a C1-C3 alkyl group; R6 represents a C1-C4 alkyl group, a C3-C6 cycloalkyl group, or the like; R7, R8, and R9 each represents a hydrogen atom, a halogen atom, or the like; R10 represents a C1-C3 alkyl group, or the like; R13 represents a C1-C3 alkyl group, or the like; and Q represents a phenyl group, or the like; has an excellent control effect on pests.

Efficient synthesis of substances related to cinacalcet hydrochloride via heck coupling

Efficient synthetic methods to process substances related to cinacalcet hydrochloride 1, generated during the preparation, were described. The compounds were identified as [1-(7,8-dihydro-naphthalen-1-yl)-ethyl]-[3-(3- trifluoromethyl-phenyl)-propyl]-amine hydrochloride 2,[1-(5,6,7,8-tetrahydro- naphthalen-1-yl)-ethyl]-[3-(3-trifluoromethyl-phenyl)-propyl]-amine hydrochloride 3 and [1-(naphthalen-2-yl)-ethyl]-[3-(3-trifluoromethyl-phenyl)- propyl]-amine hydrochloride 4. All were prepared from commercially available materials in several linear steps and characterized by their respective spectral data.