ChemicalBook Product Catalog Chemical Reagents Organic reagents The polycyclic compound 7-Methoxy-1-tetralone

7-Methoxy-1-tetralone

7-Methoxy-1-tetralone Basic information
Product Name:7-Methoxy-1-tetralone
Synonyms:7-Methoxy-1,2,3,4-tetrahydronaphthalene-1-one;7-Methoxy-1-oxotetraline;7-Methoxy-1-tetralinone;7-Methoxy-1-tetralone,97%;7-M;7-methoxytetralin-1-one;3,4-Dihydro-7-methoxy-1(2H)-naphthalenone;Methoxy-1-tetralone
CAS:6836-19-7
MF:C11H12O2
MW:176.21
EINECS:229-916-0
Product Categories:Aromatics Compounds;Butorphanol;Benzocycles;Naphthalene derivatives;Aromatics;C11 to C12;Carbonyl Compounds;Ketones;intermediates;1;bc0001
Mol File:6836-19-7.mol
7-Methoxy-1-tetralone Structure
7-Methoxy-1-tetralone Chemical Properties
Melting point 59-63 °C (lit.)
Boiling point 160-165 C
density 1.124±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Crystalline Powder
color White to beige
Water Solubility 309mg/L at 25℃
BRN 2208389
InChIKeyGABLTKRIYDNDIN-UHFFFAOYSA-N
LogP2.68
CAS DataBase Reference6836-19-7(CAS DataBase Reference)
NIST Chemistry Reference7-Methoxy-1-tetralone(6836-19-7)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
HS Code 29145090
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
7-Methoxy-1-tetralone Usage And Synthesis
Chemical PropertiesOff-White Powder
Uses7-methoxy-1-tetralone was used in the synthesis of 2,7-dimethoxy-1-tetralone, substituted derivatives of 3a,4,5,6-tetrahydrosuccinimido[3,4-b]acenaphthen-10-one and 13H-benzo[6-7]indolo[3,2-c]quinolines.
DefinitionChEBI: 7-Methoxy-3,4-dihydro-1(2H)-naphthalenone is a member of tetralins.
7-Methoxy-1-tetralone Preparation Products And Raw materials
Preparation Products7-METHOXY-1-METHYL-2-TETRALONE-->7-Methoxy-2-tetralone-->7-Hydroxy-1-tetralone-->1(2H)-Naphthalenone, 2-fluoro-3,4-dihydro-7-methoxy--->methyl 1,2,3,4-tetrahydro-7-methoxy-1-oxo-2-naphthalenecarboxylate-->1-Naphthalenol, 2-bromo-7-methoxy--->(1S)-7-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol-->salvinone
2-PROPANAMIDO-7-METHOXY-3,4-DIHYDRONAPHTHALEN-1-(2H)-ONE 1,3,5(10)-ESTRATRIEN-3,16-ALPHA, 17-BETA-TRIOL-6-ONE TRIACETATE 5-BENZYLOXY-2-CHLORO-7-METHOXY-2,3-DIHYDRO-[1,4]NAPHTHOQUINONE SALOR-INT L155381-1EA 6,7-(METHYLENEDIOXY)-1-TETRALONE 2,5,7,8-TETRAMETHOXY-2,3-DIHYDRO-[1,4]NAPHTHOQUINONE Methoxy 1,3,5(10)-ESTRATRIEN-3,17-ALPHA-DIOL-6-ONE DIACETATE 2-AMINO-3,4-DIHYDRO-7-METHOXY-2H-1-NAPHTHALENONE, HYDROCHLORIDE 2-BROMO-7-METHOXY-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE 7-METHOXY-4,4-DIMETHYL-3,4-DIHYDRO-2H-NAPHTHALEN-1-ONE SALOR-INT L155357-1EA 1,3,5(10)-ESTRATRIEN-3-OL-6,17-DIONE ACETATE SALOR-INT L155365-1EA SALOR-INT L155373-1EA SALOR-INT L155209-1EA 7-METHOXY-2-TRIFLUOROMETHYL-3,4-DIHYDRO-2H-NAPHTHALEN-1-ONE SALOR-INT L155438-1EA
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