40116-78-7

Basic information

• Product Name: 4-Morpholineethanol, a-phenyl-, (R)-
• CAS NO: 40116-78-7
• Molecular Formula: C12H17NO2
• Molecular Weight: 207.272
• Mol File: 40116-78-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 4-Morpholineethanol, a-phenyl-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Morpholineethanol, a-phenyl-, (R)-(40116-78-7)
• EPA Substance Registry System: 4-Morpholineethanol, a-phenyl-, (R)-(40116-78-7)

Safety Data

• Hazardous Substances Data: 40116-78-7(Hazardous Substances Data)

Upstream product

• 779-53-3 4-morpholinylacetophenone 
• 110-91-8 morpholine 
• 20780-53-4 (R)-Styrene oxide 
• 70-11-1 α-bromoacetophenone 
• 93-56-1 phenylethane 1,2-diol 
• 4432-34-2 2-morpholino-1-phenylethanol 
• 16355-00-3 (R)-1-phenyl-1,2-ethanediol 
• 40434-87-5 (R)-2-hydroxy-2-phenylethyl 4-methylbenzenesulfonate 

Relevant articles and documents

Synthesis of chiral alcohols by asymmetric reductions of various ketones including α-aminophenones

LiAlH4 previously treated with 2.5 equiv. of (S)-(+) or (R)-(-)-2-(2-isoindolinyl)butan-1-ol 1 reduced the six α-aminophenones 4-9 into the corresponding optically active β-aminoalcohols 10-15 whose ee's were in the range of 40-97% after chroma

AMIDO THIADIAZOLE DERIVATIVES AS NADPH OXIDASE INHIBITORS

The present invention is related to amino thiazole derivatives of Formula (I), pharmaceutical composition thereof and to their use for the treatment and/or prophylaxis of disorders or conditions related to Nicotinamide adenine dinucleotide phosphate oxidase (NADPH Oxidase).

Asymmetric self-replication of chiral 1,2-amino alcohols by highly enantioselective autoinductive reduction

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