76959-16-5

Basic information

• Product Name: Oxazole, 2-(2,3-dimethoxy-5-methylphenyl)-4,5-dihydro-4,4-dimethyl-
• CAS NO: 76959-16-5
• Molecular Formula: C14H19NO3
• Molecular Weight: 249.31
• Mol File: 76959-16-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Oxazole, 2-(2,3-dimethoxy-5-methylphenyl)-4,5-dihydro-4,4-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazole, 2-(2,3-dimethoxy-5-methylphenyl)-4,5-dihydro-4,4-dimethyl-(76959-16-5)
• EPA Substance Registry System: Oxazole, 2-(2,3-dimethoxy-5-methylphenyl)-4,5-dihydro-4,4-dimethyl-(76959-16-5)

Safety Data

• Hazardous Substances Data: 76959-16-5(Hazardous Substances Data)

Upstream product

• 5653-56-5 2,3-dimethoxy-5-methylbenzoic acid 
• 90919-49-6 2,3-Dimethoxy-5-methylbenzoyl chloride 
• 124-68-5 2-Amino-2-methyl-1-propanol 
• 80389-39-5 N-<2-(1-hydroxy-2-methylpropyl)>-2,3-dimethoxy-5-methylbenzamide 
• 107189-00-4 2-(5-Bromo-2,3-dimethoxyphenyl)-4,5-dihydro-4,4-dimethyloxazole 
• 74-88-4 methyl iodide 
• 72517-23-8 5-bromo-2,3-dimethoxybenzoic acid 
• 107188-91-0 5-bromo-2,3-dimethoxybenzoic acid chloride 
• 129117-51-7 5-Bromo-N-(2-hydroxy-1,1-dimethylethyl)-2,3-dimethoxybenzamid 
• 93-51-6 2-Methoxy-4-methylphenol 
• 5701-86-0 2,3-dimethoxy-5-methylbenzaldehyde 

Downstream Products

• 158307-79-0 4,5-dihydro-2-<2-(2',4'-dimethoxybenzyl)-3-methoxy-4-methylphenyl>-4,4'-dimethyloxazole 
• 5653-56-5 2,3-dimethoxy-5-methylbenzoic acid 
• 76959-17-6 4,4-dimethyl-2-(2-amino-3-methoxy-5-methylphenyl)-oxazoline 
• 76191-51-0 8-hydroxy-1-methoxy-3-methyl-5H-benzonaphtho<2,3-b>pyran-5,7,12-trione 
• 80389-40-8 3-methoxy-5-methyl anthranilic acid 
• 76191-50-9 Antibiotic WS-5995 C 
• 90919-49-6 2,3-Dimethoxy-5-methylbenzoyl chloride 
• 107188-76-1 (-)-(S)-N-<(1-Ethylpyrrolidin-2-yl)methyl>-2,3-dimethoxy-5-methylbenzamide 
• 127870-66-0 2-(2',4'-dimethoxybenzyl)-3-methoxy-5-methylbenzoic acid 

Relevant articles and documents

A New Synthesis of Anthraquinones Using Dihydro-oxazoles and Grignard Reagents Derived from Mg(Anthracene)(THF)3

A general synthesis of anthraquinones which depends on the displacement of the methoxy group from an o-methoxyaryldihydro-oxazole by a methoxy substituted benzylmagnesium chloride, generated by using a magnesium-anthracene complex, has been developed.The masked benzylbenzoic acids which result from these reactions are deprotected and then ring-closed to anthrones which on oxidation yield anthraquinones.In this way, the followeing naturally occurring anthraquinones (or derivatives thereof have been synthesized): chrysophanol (9), islandicin (19), digitopurpone (21), tri-O-methylemodin (26), and di-O-methylsoranjidiol (29).

Structure and synthesis of new anticoccidial antibiotics isolated from Streptomyces auranticolor

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STRUCTURE ELUCIDATION AND SYNTHESIS OF A NEW ANTICOCCIDICAL SUBSTANCE ISOLATED FROM STREPTOMYCES AURANTICOLOR

The structure elucidation and synthesis of WS 5995, produced by Streptomyces auranticolor, were described.