51632-31-6

Basic information

• Product Name: 2-(4-Methoxyphenyl)-3-Methylbutanoic acid
• Synonyms: 2-(4-Methoxyphenyl)-3-Methylbutanoic acid;Benzeneacetic acid, 4-methoxy-±-(1-methylethyl)-
• CAS NO: 51632-31-6
• Molecular Formula: C₁₂H₁₆O₃
• Molecular Weight: 208.25364
• Mol File: 51632-31-6.mol
• Article Data: 9

Chemical Properties

• Melting Point: 153-156 °C
• Boiling Point: 330.6°Cat760mmHg
• Flash Point: 123.3°C
• Appearance: /
• Density: 1.087g/cm³
• Vapor Pressure: 6.59E-05mmHg at 25°C
• Refractive Index: 1.516
• PKA: 4.41±0.10(Predicted)
• CAS DataBase Reference: 2-(4-Methoxyphenyl)-3-Methylbutanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Methoxyphenyl)-3-Methylbutanoic acid(51632-31-6)
• EPA Substance Registry System: 2-(4-Methoxyphenyl)-3-Methylbutanoic acid(51632-31-6)

Safety Data

• Hazardous Substances Data: 51632-31-6(Hazardous Substances Data)

Usage

Classification

Nonsteroidal anti-inflammatory drug (NSAID) This categorizes the compound as a medication used to relieve pain and reduce inflammation.

Mechanism of action

Inhibition of prostaglandin production The compound works by inhibiting the production of prostaglandins, which are responsible for causing pain and inflammation in the body.

Administration route

Oral The compound is typically taken by mouth for its therapeutic effects.

Medical uses

Treatment of conditions like arthritis and menstrual pain The compound is used to alleviate pain and inflammation associated with these conditions.

Potential side effects

Stomach irritation, dizziness, and headache These are some of the possible adverse effects that may occur while using the compound.

Importance of supervision

Use under the guidance of a healthcare professional To minimize the risk of adverse effects, it is crucial to use this compound under the supervision of a medical professional.

InChI:InChI=1/C12H16O3/c1-8(2)11(12(13)14)9-4-6-10(15-3)7-5-9/h4-8,11H,1-3H3,(H,13,14)

Upstream product

• 51632-18-9 2-(4-methoxyphenyl)-3-methylbutyronitrile 
• 75-30-9 2-iodo-propane 
• 104-01-8 4-Methoxyphenylacetic acid 
• 107-21-1 ethylene glycol 
• 104-47-2 p-methoxybenzylnitrile 
• 14062-18-1 ethyl p-methoxyphenylacetate 
• 75-26-3 isopropyl bromide 
• 54656-96-1 (S)-1-(4-pyridyl)ethanol 
• 67794-93-8 C₂₄H₃₀O₅ 

Downstream Products

• 51629-20-0 3'-benzylbenzyl α-isopropyl-p-methoxyphenylacetate 
• 51628-91-2 2-(4-Methoxy-phenyl)-3-methyl-butyric acid 1-(3,4-dichloro-phenyl)-prop-2-ynyl ester 
• 51628-95-6 3'-Phenoxybenzyl-α-isopropyl-4-methoxy-phenylacetat 
• 51631-32-4 2-(4-methoxyphenyl)-3-methylbutanoyl chloride 
• 80607-79-0 2-(4-Methoxy-3-nitrophenyl)-3-methylbuttersaeure 
• 131691-09-3 2-(4-Methoxy-phenyl)-3-methyl-butyric acid 2-(2-methyl-5-nitro-imidazol-1-yl)-ethyl ester 
• 80607-62-1 N-Butyl-2-(4-methoxyphenyl)-3-methylbutyramid 
• 344270-05-9 2-(4-Methoxy-3-nitro-phenyl)-3-methyl-butyryl chloride 
• 80607-63-2 N-Butyl-2-(4-methoxy-3-nitrophenyl)-3-methylbutyramid 
• 74569-39-4 α-Fluoro-3-phenoxybenzyl α-isopropyl-(4-methoxyphenyl)acetate 
• 945666-90-0 4-methoxyphenyl isopropyl ketene 

Relevant articles and documents

Preparation of aryl alkyl ketenes

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Highly enantioselective direct alkylation of arylacetic acids with chiral lithium amides as traceless auxiliaries

A direct, highly enantioselective alkylation of arylacetic acids via enediolates using a readily available chiral lithium amide as a stereodirecting reagent has been developed. This approach circumvents the traditional attachment and removal of chiral auxiliaries used currently for this type of transformation. The protocol is operationally simple, and the chiral reagent is readily recoverable.

Optisch aktive α-Arylcarbonsaeuren durch kinetische Enantiomerentrennung: Pyrethroidsaeuren

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