128223-59-6

Basic information

• Product Name: 1,3-Propanediol, 2-(phenylmethoxy)-, acetate 4-methylbenzenesulfonate, (R)-
• CAS NO: 128223-59-6
• Molecular Formula: C19H22O6S
• Molecular Weight: 378.446
• Mol File: 128223-59-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-Propanediol, 2-(phenylmethoxy)-, acetate 4-methylbenzenesulfonate, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Propanediol, 2-(phenylmethoxy)-, acetate 4-methylbenzenesulfonate, (R)-(128223-59-6)
• EPA Substance Registry System: 1,3-Propanediol, 2-(phenylmethoxy)-, acetate 4-methylbenzenesulfonate, (R)-(128223-59-6)

Safety Data

• Hazardous Substances Data: 128223-59-6(Hazardous Substances Data)

Upstream product

• 14690-00-7 2-O-benzylglycerol 
• 109429-01-8 (S)-2-(benzyloxy)-3-hydroxypropyl acetate 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 119870-22-3 (S)-2-benzyloxy-3-isopropylamino-1-propanol 
• 119870-21-2 ((S)-2-Benzyloxy-3-chloro-propyl)-isopropyl-amine 
• 146797-75-3 (R)-2-O-benzyl-3-O-tetrahydropyranyl-1-O-tosylglycerol 
• 146923-48-0 (S)-2-O-benzyl-3-O-hexadecyl-1-O-tetrahydropyranylglycerol 
• 41274-09-3 (R)-3-tosyloxy-1,2-propanediol 
• 119870-20-1 (R)-(-)-3-tosyloxy-2-benzyloxy-1-propanol 

Relevant articles and documents

Synthesis of optically active lipopeptide analogs from the outer membrane of Escherichia coli

The synthesis of optically active lipopeptide derivatives has been accomplished by the use of chiral glycerol derivatives. Lipopeptide derivatives with (R)-glycerol moieties showed higher mitogenic activities than those with the (S)-configuration. N-2,2,2-Trichloroethoxycarbonyl lipopeptide derivatives increased mitogenic activity.

HIGHLY EFFICIENT LIPASE-CATALYZED ASYMMETRIC SYNTHESIS OF CHIRAL GLYCEROL DERIVATIVES LEADING TO PRACTICAL SYNTHESIS OF (S)-PROPRANOLOL

Efficient asymmetric synthesis of chiral glycerol derivatives was realized by lipase-catalyzed reaction in organic medium and its application for synthesis of (S)-propranolol was demostrated.