6-methoxy-1-tetralone

6-methoxy-1-tetralone Basic information
Product Name:6-methoxy-1-tetralone
Synonyms:6-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALEN-1-ONE;6-METHOXY-1,2,3,4-TETRAHYDRO-1-NAPHTHALENONE;6-METHOXY-1,2,3,4-TETRAHYDRO-1-NAPHTHONE;6-METHOXY-3,4-DIHYDRO-2H-NAPHTHALEN-1-ONE;6-METHOXY-1-TETRALONE;6-METHOXY TETRALONE;6-METHOXY-ALPHA-TETRALONE;TIMTEC-BB SBB007549
CAS:1078-19-9
MF:C11H12O2
MW:176.21
EINECS:214-078-0
Product Categories:Ketone;C11 to C12;Carbonyl Compounds;Carbonyl Compounds;Ketones
Mol File:1078-19-9.mol
6-methoxy-1-tetralone Structure
6-methoxy-1-tetralone Chemical Properties
Melting point 77-79 °C (lit.)
Boiling point 171 °C/11 mmHg (lit.)
density 1.0558 (rough estimate)
refractive index 1.5250 (estimate)
Fp 171°C/11mm
storage temp. Sealed in dry,Room Temperature
form Fine Crystalline Powder
color Yellow to light brown
PH5.96 at 23℃ and 10g/L
Merck 14,6000
BRN 972739
InChIKeyMNALUTYMBUBKNX-UHFFFAOYSA-N
CAS DataBase Reference1078-19-9(CAS DataBase Reference)
NIST Chemistry Reference1(2H)-Naphthalenone, 3,4-dihydro-6-methoxy-(1078-19-9)
EPA Substance Registry System1(2H)-Naphthalenone, 3,4-dihydro-6-methoxy- (1078-19-9)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-20/21/22
Safety Statements 24/25-36-26
WGK Germany 3
Hazard Note Irritant
TSCA Yes
HS Code 29145000
MSDS Information
ProviderLanguage
6-Methoxytetralone English
SigmaAldrich English
ACROS English
ALFA English
6-methoxy-1-tetralone Usage And Synthesis
Chemical Propertiesyellow to light brown fine crystalline powder
Uses6-Methoxy-1-tetralone is a reagent useful in the synthesis of (2-(furanyl)vinyl)-1-tetralone chalcones which possesses anticancer agents and inducers of apoptosis.
DefinitionChEBI: 6-Methoxy-1-tetralone is a member of tetralins.
Synthesis Reference(s)Journal of the American Chemical Society, 64, p. 94, 1942 DOI: 10.1021/ja01253a025
Tetrahedron Letters, 9, p. 2917, 1968 DOI: 10.1016/S0040-4039(00)89611-2
Synthesis The synthesis of 6-methoxy-1-tetralone is as follows:Eaton's reagent (1.00 mL, 5.31 mmol) was added slowly to a stirred solution of methyl 4-(3-methoxyphenyl)butanoate (4; 0.37g, 1.78 mmol) in DCE (1 mL). The resulting mixture was stirred at 75 °C for 2h under N2 atmosphere. Then, the reaction mixture was allowed to reach room temperature, and was poured over ice-water and extracted with EtOAc (3 × 15 mL). The combined organic extracts were washed successively with brine (2 × 15 mL) and H2O (2 × 20 mL), filtered over Na2SO4 and concentrated under reduced pressure. The resulting brownish oil was fractionated by column chromatography (silica gel, EtOAc-hexanes, 1:9) to obtain 6-methoxy-1-tetralone as ayellowish oil; yield: 0.28 g (91%).    1078-19-9.png
(-)-3-Methoxy-17-methyl-10-oxomorphinan 6-methoxy-1-tetralone 6-[(5-THIEN-2-YLPYRIMIDIN-2-YL)OXY]-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE 6,7-Dimethoxy-1-tetralone Nabumetone 6,7-(METHYLENEDIOXY)-1-TETRALONE SALOR-INT L155179-1EA 6-[(5-BROMOPYRIMIDIN-2-YL)OXY]-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE Methoxy 3-(1,2,3,4-Tetrahydro-6-methoxy-1-oxo-2-naphthoyl)propionicacid 7-Methoxy-1-tetralone (Trifluoromethoxy)benzene SALOR-INT L155306-1EA SALOR-INT L155195-1EA dactylocycline B SALOR-INT L155187-1EA 1-Tetralone 3,11-DIMETHOXY-7-PHENYL-6,8,9,13B-TETRAHYDRO-5H-DIBENZO[C,H]XANTHYLIUM PERCHLORATE

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