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1-[(2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-ethanone

Base Information
  • Chemical Name:1-[(2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-ethanone
  • CAS No.:41098-96-8
  • Molecular Formula:C14H18O4
  • Molecular Weight:250.295
  • Hs Code.:
  • Mol file:41098-96-8.mol
1-[(2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-ethanone

Synonyms:(-)-2(R)-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2(R)-naphthol;1-[(2R)-1,2,3,4-tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-Ethanone Aglycone Anticancer API interMediate;(R)-(-)-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphtol;(-)-PGE1 methyl ester;(R)-(-)-2-acetyl-1,2,3,4-tetrahydro-5,8-dimethoxy-2-naphthol;(R)-(-)-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol;

Suppliers and Price of 1-[(2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-ethanone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Chemenu
  • (R)-1-(2-hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl)ethan-1-one 97%
  • 1g
  • $ 1664.00
Total 6 raw suppliers
Chemical Property of 1-[(2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-ethanone
Chemical Property:
  • Melting Point:128-129℃ (ethyl ether hexane ) 
  • PSA:55.76000 
  • Density:1.186±0.06 g/cm3 (20 oC 760 Torr) 
  • LogP:1.51260 
Purity/Quality:

98%Min *data from raw suppliers

(R)-1-(2-hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl)ethan-1-one 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • General Description 1-[(2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-ethanone, also known as (R)-(-)-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol, is a key chiral intermediate in the synthesis of anthracycline antibiotics and anthracyclinones. It can be prepared enantioselectively via hydroxylation of a potassium enolate using an N-sulfonyloxaziridine or through Sharpless asymmetric dihydroxylation followed by regioselective transformations, yielding the compound with high enantiomeric excess (>95% ee) and satisfactory overall yields (35–52%). Its synthesis is notable for efficiency and minimal purification requirements.
Technology Process of 1-[(2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-ethanone

There total 62 articles about 1-[(2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxy-2-naphthalenyl]-ethanone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

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