103234-38-4

Basic information

• Product Name: 4-(3,5-DIMETHYL-4-METHOXYPHENYL)-4-OXOBUTYRIC ACID
• Synonyms: 4-(3,5-DIMETHYL-4-METHOXYPHENYL)-4-OXOBUTYRIC ACID
• CAS NO: 103234-38-4
• Molecular Formula: C₁₃H₁₆O₄
• Molecular Weight: 236.26
• Mol File: 103234-38-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 440.7°C at 760 mmHg
• Flash Point: 168.9°C
• Appearance: /
• Density: 1.151g/cm³
• Vapor Pressure: 1.52E-08mmHg at 25°C
• Refractive Index: 1.53
• CAS DataBase Reference: 4-(3,5-DIMETHYL-4-METHOXYPHENYL)-4-OXOBUTYRIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3,5-DIMETHYL-4-METHOXYPHENYL)-4-OXOBUTYRIC ACID(103234-38-4)
• EPA Substance Registry System: 4-(3,5-DIMETHYL-4-METHOXYPHENYL)-4-OXOBUTYRIC ACID(103234-38-4)

Safety Data

• Hazardous Substances Data: 103234-38-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H16O4/c1-8-6-10(7-9(2)13(8)17-3)11(14)4-5-12(15)16/h6-7H,4-5H2,1-3H3,(H,15,16)

Upstream product

• 108-30-5 succinic acid anhydride 
• 1004-66-6 2-methoxy-1,3-dimethylbenzene 

Downstream Products

• 109025-27-6 4-(4-methoxy-3,5-dimethylphenyl)butanoic acid 
• 948995-56-0 4-(4-methoxy-3,5-dimethylphenyl)-4-oxobutyric acid methyl ester 
• 948995-62-8 4-[3,5-dimethyl-4-(4-nitro-benzyloxy)-phenyl]-4-oxo-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 1012794-99-8 C₁₉H₁₉NO₆ 
• 948995-63-9 N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide 
• 948995-75-3 C₄₀H₄₉N₅O₁₆ 
• 948995-77-5 C₅₂H₆₅N₅O₂₄ 
• 948995-57-1 4-[3,5-dimethyl-4-(4-nitro-benzyloxy)-phenyl]-4-oxo-butyric acid methyl ester 
• 52246-10-3 4-(4-hydroxy-3,5-dimethylphenyl)-4-oxobutyric acid methyl ester 

Relevant articles and documents

Design, Conformation, and Crystallography of 2-Naphthyl Phenyl Ethers as Potent Anti-HIV Agents

Catechol diethers that incorporate a 7-cyano-2-naphthyl substituent are reported as non-nucleoside inhibitors of HIV-1 reverse transcriptase (NNRTIs). Many of the compounds have 1-10 nM potencies toward wild-type HIV-1. An interesting conformational effect allows two unique conformers for the naphthyl group in complexes with HIV-RT. X-ray crystal structures for 4a and 4f illustrate the alternatives.

Cyclohexane-1,3-dione derivatives, compositions containing them, processes for preparing them, and their use as herbicides and plant growth regulators

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