CAS 23981-80-8
:(±)-Naproxen
- (RS)-Naproxen
- (±)-2-(6-Methoxy-2-naphthalenyl)propionic acid
- (±)-6-Methoxy-α-methyl-2-naphthaleneacetic acid
- (±)-Naproxen
- 2-(6-Methoxy-2-naphthyl)propanoic acid
- 2-(6-Methoxynaphthalen-2-yl)propanoic acid
- 2-(6-Methoxynaphthalen-2-yl)propionic acid
- 2-Naphthaleneacetic acid, 6-methoxy-α-methyl-
- 6-Methoxy-2-naphthyl-α-methylacetic acid
- <span class="text-smallcaps">D</smallcap><smallcap>L</span>-2-(6-Methoxy-2-naphthyl)propionic acid
- <span class="text-smallcaps">D</smallcap><smallcap>L</span>-Naproxen
- DL-Naproxen
- Racemic Naproxen
- α-(6-Methoxy-2-naphthyl)propionic acid
- See more synonyms
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(+/-)-Naproxen
CAS:Formula:C14H14O3Purity:>98.0%(GC)(T)Color and Shape:White to Light red to Green powder to crystalMolecular weight:230.262-(6-Methoxynaphthalen-2-Yl)Propanoic Acid
CAS:2-(6-Methoxynaphthalen-2-Yl)Propanoic AcidFormula:C14H14O3Purity:98%Color and Shape:SolidMolecular weight:230.26(+/-)-Naproxen-d3 (α-methyl-d3)
CAS:Purity:99 atom % DColor and Shape:White SolidMolecular weight:233.282-(6-Methoxynaphthalen-2-Yl)Propanoic Acid
CAS:Formula:C14H14O3Purity:98%Color and Shape:SolidMolecular weight:230.2592rac-Naproxen
CAS:Applications An anti-inflammatory, analgesic, antipyretic. A non-steroidal anti-inflammatory.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Harrison, I.T., et al.: J. Med. Chem., 13, 203 (1970)Formula:C14H14O3Color and Shape:NeatMolecular weight:230.262-(6-Methoxy-2-naphthyl)propionic acid
CAS:Formula:C14H14O3Purity:97%Color and Shape:SolidMolecular weight:230.263(±)-Naproxen
CAS:2-(6-Methoxynaphthalen-2-yl)propanoic acidFormula:C14H14O3Purity:98%Molecular weight:230.26rac-Naproxen-13C3
CAS:Controlled ProductFormula:C3C11H14O3Color and Shape:NeatMolecular weight:233.237rac-Naproxen
CAS:Naproxen is a non-steroidal anti-inflammatory drug that is used to treat pain, fever, and inflammation. It is an analgesic and antipyretic agent. Naproxen has been shown to have a high affinity for copper chloride, which may be due to the formation of an amide bond. The reaction mechanism of naproxen's inhibition of prostaglandin synthesis in bacteria has been investigated using x-ray diffraction data from bacterial strains and human serum. Naproxen also has inhibitory properties on the reaction solution in vitro and enhances the toxicity studies with isooctane in vivo.
Formula:C14H14O3Purity:(%) Min. 95%Color and Shape:White/Off-White SolidMolecular weight:230.26 g/mol













