128821-01-2

Basic information

• Product Name: (R)-(+)-1-BENZYLOXY-BUTANE-2-OL
• Synonyms: (R)-(+)-1-BENZYLOXY-BUTANE-2-OL;(R)-(+)-1-BENZYLOXYBUTAN-2-OL
• CAS NO: 128821-01-2
• Molecular Formula: C11H16O2
• Molecular Weight: 180.24
• Mol File: 128821-01-2.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 280.7 °C at 760 mmHg
• Flash Point: 114 °C
• Appearance: /
• Density: 1.023 g/cm³
• CAS DataBase Reference: (R)-(+)-1-BENZYLOXY-BUTANE-2-OL(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(+)-1-BENZYLOXY-BUTANE-2-OL(128821-01-2)
• EPA Substance Registry System: (R)-(+)-1-BENZYLOXY-BUTANE-2-OL(128821-01-2)

Safety Data

• Hazardous Substances Data: 128821-01-2(Hazardous Substances Data)

Usage

General Description

(R)-(+)-1-benzyloxy-butane-2-ol is a chemical compound with the molecular formula C11H16O2. It is a chiral compound, meaning it has a non-superimposable mirror image, and the (R)-enantiomer is the active form. (R)-(+)-1-BENZYLOXY-BUTANE-2-OL is commonly used as a building block for the synthesis of various pharmaceuticals and organic compounds. It is also used as a chiral auxiliary in asymmetric synthesis reactions. The benzyloxy group in the compound provides protection for hydroxyl groups in organic synthesis and can be selectively removed under specific conditions. Its versatile chemical properties and applications make it a valuable compound in the field of organic chemistry.

Upstream product

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Downstream Products

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Relevant articles and documents

Diastereoselective Synthesis of Functionalized 9-Ring Ethers (Oxonins).

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Copper(I)-catalyzed asymmetric desymmetrization: Synthesis of five-membered-ring compounds containing all-carbon quaternary stereocenters

A highly stereoselective catalytic alkylation sequence for the synthesis of highly functionalized and versatile five-membered-ring compounds bearing all-carbon quaternary stereocenters was developed. Enantioselective desymmetrization of achiral cyclopentene-1,3-diones was thus executed by chiral Cu-phosphoramidite catalysts. A variety of complicated cyclopentane derivatives can be synthesized with excellent stereoselectivities using a low catalyst loading in a one-pot operation.