199991-74-7

Basic information

• Product Name: 2-((S)-2-Benzyloxy-1-methyl-ethoxy)-propan-1-ol
• CAS NO: 199991-74-7
• Molecular Weight: 224.3
• Mol File: 199991-74-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-((S)-2-Benzyloxy-1-methyl-ethoxy)-propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((S)-2-Benzyloxy-1-methyl-ethoxy)-propan-1-ol(199991-74-7)
• EPA Substance Registry System: 2-((S)-2-Benzyloxy-1-methyl-ethoxy)-propan-1-ol(199991-74-7)

Safety Data

• Hazardous Substances Data: 199991-74-7(Hazardous Substances Data)

Upstream product

• 85483-96-1 (2S)-1-benzyloxy-2-propanyl tetrahydropyran-2-yl ether 
• 13807-91-5 (2S)-1-(benzyloxy)propan-2-ol 

Downstream Products

• 188303-41-5 (5S,8S,10S,13S)-19,21-Dimethoxy-8,10-dimethyl-5,13-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-triene 
• 199991-92-9 (5R,8S,10S,13R)-19,21-Dimethoxy-8,10-dimethyl-5,13-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-triene 
• 188303-42-6 (5S,8S,10S,13S)-19-Methoxy-8,10-dimethyl-5,13-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-trien-21-ol 
• 199991-96-3 (5R,8S,10S,13R)-19-Methoxy-8,10-dimethyl-5,13-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-trien-21-ol 
• 199992-19-3 (5S,8S,10S,13S)-8,10-Dimethyl-5,13-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17-diene-19,21-dione 
• 199992-24-0 (5R,8S,10S,13R)-8,10-Dimethyl-5,13-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17-diene-19,21-dione 
• 171753-73-4 (2S,2'S)-oxybis(propane-2,1-diyl)bis(4-methylbenzenesulfonate) 

Relevant articles and documents

Preparation of optically active azophenolic crown ethers containing 1-phenylethane-1,2-diol and 2,4-dimethyl-3-oxapentane-1,5-diol as a chiral subunit: Temperature-dependent enantiomer selectivity in the complexation with chiral amines

With (2S,4S)-2,4-dimethyl-3-oxapentane-1,5-diol and (S)- or (R)-1-phenylethane-1,2-diol as chiral subunits, optically active azophenolic crown ethers (S,S,S,S)-1, (R,S,S,R)-2, (S,S,S,S)-3 and (R,S,S,R)-4 possessing two phenyl and two methyl substituents together with the p-(2,4-dinitrophenylazo)phenol moiety have been prepared in enantiomerically pure forms. Temperature-dependent enantiomer selectivity in the complexation of these crown ethers with chiral amines has been studied by the UV-visible spectroscopic method in chloroform and from the observed association constants, thermodynamic parameters for the complexation have been calculated.