4,4'-Dimethoxybiphenyl

4,4'-Dimethoxybiphenyl
  • CAS No.:2132-80-1

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
Other grades of this product :
4,4'-Dimethoxybiphenyl Basic information
Product Name:4,4'-Dimethoxybiphenyl
Synonyms:4,4'-BIANISOLE;4,4'-DIMETHOXYBIPHENYL;4,4'-Dimethoxy-1,1'-biphenyl;4,4'-Dimethoxybiphenyl,98%;4,4'-Dimethyoxybiphenyl;4,4′-Dimethoxybiphenyl,4,4′-Bianisole;Biphenyl, 4,4'-dimethoxy- (6CI,7CI,8CI);4,4'-DiMethoxylbiphenyl
CAS:2132-80-1
MF:C14H14O2
MW:214.26
EINECS:
Product Categories:Biphenyl & Diphenyl ether
Mol File:2132-80-1.mol
4,4'-Dimethoxybiphenyl Chemical Properties
Melting point 179-180 °C (subl.)(lit.)
Boiling point 314.4°C (rough estimate)
density 1.0781 (rough estimate)
refractive index 1.5570 (estimate)
InChIKeyUIMPAOAAAYDUKQ-UHFFFAOYSA-N
CAS DataBase Reference2132-80-1(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
4,4'-Dimethoxybiphenyl Usage And Synthesis
Chemical Propertieslight yellow shiny flakes
Uses4,4′-Dimethoxybiphenyl was used to study the coupled methyl-group rotation and methoxy-group libration.
Synthesis Reference(s)Journal of the American Chemical Society, 94, p. 4780, 1972 DOI: 10.1021/ja00768a084Organic Syntheses, Coll. Vol. 6, p. 468, 1988Tetrahedron Letters, 13, p. 2271, 1972

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