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Catalog Number:
16594
CAS Number:
3966-32-3
(R-(-)-α-Methoxyphenylacetic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
O-Methyl-(R-mandelic acid
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Product Information

(R)-(-)-a-Methoxyphenylacetic acid is a valuable chiral building block widely utilized in the synthesis of pharmaceuticals and agrochemicals. This compound is recognized for its unique ability to enhance the efficacy of various drug formulations, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and analgesics. Its chiral nature allows for the production of enantiomerically pure compounds, which is crucial in the pharmaceutical industry to ensure optimal therapeutic effects and minimize side effects.

In addition to its pharmaceutical applications, (R)-(-)-a-Methoxyphenylacetic acid serves as an important intermediate in organic synthesis, enabling researchers to create complex molecules with precision. Its favorable solubility characteristics and stability under various conditions make it an ideal candidate for use in diverse chemical reactions. This compound not only streamlines the synthesis process but also enhances the overall yield and purity of the final products, making it a preferred choice for both academic research and industrial applications.

Synonyms
O-Methyl-(R-mandelic acid
CAS Number
3966-32-3
Purity
≥ 99% (HPLC)
Molecular Formula
C9H10O3
Molecular Weight
166.17
MDL Number
MFCD00004250
PubChem ID
107202
Melting Point
64-69 ºC
Appearance
Off-white solid
Optical Rotation
[a]D20 - 159 ± 2 º
Conditions
Store at 0-8°C
General Information
Synonyms
O-Methyl-(R-mandelic acid
CAS Number
3966-32-3
Purity
≥ 99% (HPLC)
Molecular Formula
C9H10O3
Molecular Weight
166.17
MDL Number
MFCD00004250
PubChem ID
107202
Melting Point
64-69 ºC
Appearance
Off-white solid
Optical Rotation
[a]D20 - 159 ± 2 º
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-(-)-a-Methoxyphenylacetic acid is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic medications.
  • Chiral Synthesis: Its chiral nature makes it valuable in asymmetric synthesis, allowing chemists to create specific enantiomers that are crucial for drug efficacy and safety.
  • Biochemical Research: Researchers use this compound to study its effects on biological systems, helping to elucidate mechanisms of action for various biochemical pathways.
  • Cosmetic Industry: It is also explored in cosmetic formulations for its potential skin-soothing properties, providing a natural alternative to synthetic additives.
  • Analytical Chemistry: The compound is employed as a standard in analytical methods, aiding in the quantification and analysis of similar compounds in complex mixtures.

Citations