98704-78-0

Basic information

• Product Name: [5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-pyridin-2-yl]-methanol
• Synonyms: [5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-pyridin-2-yl]-methanol
• CAS NO: 98704-78-0
• Molecular Weight: 298.342
• Mol File: 98704-78-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-pyridin-2-yl]-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-pyridin-2-yl]-methanol(98704-78-0)
• EPA Substance Registry System: [5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-pyridin-2-yl]-methanol(98704-78-0)

Safety Data

• Hazardous Substances Data: 98704-78-0(Hazardous Substances Data)

Upstream product

• 98704-76-8 5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-2-methyl-pyridine 1-oxide 
• 98704-75-7 5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-2-methyl-pyridine 
• 81659-59-8 5-oxazolinyl-2-methylpyridine 
• 81659-47-4 ((4S,5S)-5-Phenyl-2-pyridin-3-yl-4,5-dihydro-oxazol-4-yl)-methanol 
• 56624-12-5 ethyl (3-pyridyl)imidate dihydrochloride 
• 28143-91-1 (1S,2S)-2-amino-1-phenyl-1,3-diol 
• 98704-77-9 Acetic acid 5-((4S,5S)-4-methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-pyridin-2-ylmethyl ester 

Downstream Products

• 98704-91-7 2-[5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-pyridin-2-ylmethoxy]-1-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-ethanone 

Relevant articles and documents

Nicotinic Acid Lariat Ethers: Syntheses, Complexation, and Reduction

Combination of 2-(hydroxymethyl)-5-oxazolinylpyridine 16a with lariat ethers 21 and 23 generated chiral 6-methylnicotinic oxazoline lariat ethers 22 and 24, respectively.Chiral lariat ether 24b by stereoselective metal-directed addition of methylmagnesium bromide was converted to the corresponding enantiomerically enriched N-magnesio-1,4-dihydropyridine 26.Lariat 26 and the nonlariat analogue 31 both reduced α,α,α-trifluoroacetophenone in a NADH model-like reduction to give the S alcohol 32 in low enantiomeric excess.