50706-29-1

Basic information

• Product Name: 5-Isopropyl-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester
• CAS NO: 50706-29-1
• Molecular Weight: 247.294
• Mol File: 50706-29-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-Isopropyl-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Isopropyl-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester(50706-29-1)
• EPA Substance Registry System: 5-Isopropyl-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester(50706-29-1)

Safety Data

• Hazardous Substances Data: 50706-29-1(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 5817-22-1 (2RS,3RS)-2-amino-3-hydroxy-4-methylpentanoic acid 
• 98-88-4 benzoyl chloride 

Downstream Products

• 133071-07-5 rac-erythro-3-Hydroxyleucin-N-sulfamat Natriumsalz 
• 5817-22-1 D,L-erythro β-Hydroxyleucine 

Relevant articles and documents

Isolation and Structure Elucidation of Ergokonin A and B; Two New Antifungal Sterol Antibiotics from Trichoderma koningii

Isolation and structure elucidation by 2D-NMR spectroscopy of the two new antifungal sterol antibiotics ergokonin A (1) and B (2a) from Trichoderma koningii are described.The structures of 1 and 2a are derived from ergosterol and characterized by an 18-carboxy group.In addition ergokonin A (1) is esterified at the 3-hydroxy group with (2S,3S)-3-hydroxyleucine 3-O-sulfate (3c).In the course of structure elucidation of the amino acid residue the stereoisomers of 3-hydroxyleucine N-sulfamate and 3-O-sulfate (3b, c) have been synthesized and characterized by NMR spectroscopy.