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Postion:Product Catalog >Chemical Reagents>Organic reagents>The polycyclic compound>6-methoxy-1-tetralone
6-methoxy-1-tetralone
  • 6-methoxy-1-tetralone
  • 6-methoxy-1-tetralone
  • 6-methoxy-1-tetralone
  • 6-methoxy-1-tetralone
  • 6-methoxy-1-tetralone

6-methoxy-1-tetralone NEW

Price Get Latest Price
Package 25KG
Min. Order: 1KG
Supply Ability: 50000KG/month
Update Time: 2023-08-16

Product Details

Product Name: 6-methoxy-1-tetralone CAS No.: 1078-19-9
EC-No.: 214-078-0 Min. Order: 1KG
Purity: 99% Supply Ability: 50000KG/month
Release date: 2023/08/16

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
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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)
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
SynthesisThe 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%).    Article illustration

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Packing &shipping&Payment

Packing:25kg/drum
Shipping:by sea or by air
Payment:T/T,western union,moneygram
Packaging Details drum
Port:Tianjin
Lead Time :
Quantity(Kilograms)1 - 10000>10000
Est. Time(days)5To be negotiated

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Article illustrationCompany information
Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in 4'-Methylacetophenone,Levamisole hydrochloride ,N-Methylformamide and other chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.

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