109371-31-5

Basic information

• Product Name: (R)-(+)-1-BENZOYLOXY-2-BENZYLOXY-3-TOSYLOXYPROPANE
• Synonyms: (R)-(+)-1-BENZOYLOXY-2-BENZYLOXY-3-TOSYLOXYPROPANE;1,3-Propanediol, 2-(phenylmethoxy)-, benzoate 4-methylbenzenesulfonate, (R)-;(R)-(+)-1-BENZOYLOXY-2-BENZYLOXY-3-TOSYLOXYPROPANE 99+%;(R)-2-(Benzyloxy)-3-(tosyloxy)propyl benzoate
• CAS NO: 109371-31-5
• Molecular Formula: C₂₄H₂₄O₆S
• Molecular Weight: 440.51
• Mol File: 109371-31-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 585.9±50.0 °C(Predicted)
• Appearance: /
• Density: 1.247±0.06 g/cm3(Predicted)
• Refractive Index: 1.584
• CAS DataBase Reference: (R)-(+)-1-BENZOYLOXY-2-BENZYLOXY-3-TOSYLOXYPROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(+)-1-BENZOYLOXY-2-BENZYLOXY-3-TOSYLOXYPROPANE(109371-31-5)
• EPA Substance Registry System: (R)-(+)-1-BENZOYLOXY-2-BENZYLOXY-3-TOSYLOXYPROPANE(109371-31-5)

Safety Data

• Safety Statements: S22:Do not inhale dust.; S24/25:Avoid contact with skin and eyes.
• Hazardous Substances Data: 109371-31-5(Hazardous Substances Data)

Usage

General Description

(R)-(+)-1-Benzyloxy-2-benzyloxy-3-tosyloxypropane, also known as benzyl glycidyl ether tosylate, is a chemical compound with a molecular formula C26H24O7S. It is a highly versatile and reactive compound that is commonly used in organic synthesis as a protecting group for alcohols and as a precursor for the synthesis of various pharmaceuticals and biologically active molecules. The compound is often employed in the production of complex molecular structures and has found applications in the field of medicinal chemistry and drug development. Additionally, it is known for its ability to undergo various chemical transformations, making it a valuable building block in the synthesis of organic compounds.

InChI:InChI=1/C24H24O6S/c1-19-12-14-23(15-13-19)31(26,27)30-18-22(28-16-20-8-4-2-5-9-20)17-29-24(25)21-10-6-3-7-11-21/h2-15,22H,16-18H2,1H3/t22-/m1/s1

Upstream product

• 109371-34-8 Benzoic acid (S)-3-acetoxy-2-benzyloxy-propyl ester 
• 105409-40-3 1,3-di-O-propionyl-2-O-benzylglycerol 
• 109429-00-7 <(R)-2-(benzyloxy)-3-hydroxypropyl> acetate 
• 105409-38-9 1,3-di-O-acetyl-2-O-benzylglycerol 
• 109430-97-9 (-)-2-(benzyloxy)-3-hydroxypropyl benzoate 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

ENANTIOMERENREINE GLYCERIN-DERIVATE DURCH ENZYMATISCHE HYDROLYSE PROCHIRALER ESTER

A practical method for large scale preparation of optical active glycerols protected in a versatile manner is described herein.Among these the crystalline pure enantiomers V deserve highest attention, since they offer three different functionalities for s