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1123787-01-8

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1123787-01-8 Usage

Description

[(3R)-3-fluorooxolan-3-yl]Methanol is a fluorinated organic compound with the molecular formula C5H9FO2. It features a five-membered oxolan ring with a fluorine substituent, attached to a methanol group. This unique structure and the presence of a fluorine atom may endow it with special properties, making it a promising candidate for various applications in organic synthesis, pharmaceuticals, and materials science.

Uses

Used in Organic Synthesis:
[(3R)-3-fluorooxolan-3-yl]Methanol is used as a building block or intermediate in organic synthesis for the development of new compounds with potential applications in various fields. Its unique structure and fluorine atom can be utilized to create novel molecules with desired properties.
Used in Pharmaceuticals:
[(3R)-3-fluorooxolan-3-yl]Methanol is used as a pharmaceutical intermediate for the synthesis of drug candidates. The presence of the fluorine atom and the oxolan ring can contribute to the biological activity and pharmacokinetic properties of the resulting compounds, potentially leading to the discovery of new therapeutic agents.
Used in Materials Science:
[(3R)-3-fluorooxolan-3-yl]Methanol is used as a component in the development of new materials with specific properties. Its unique structure and fluorine atom can be incorporated into polymers, coatings, or other materials to enhance their performance, stability, or other characteristics.
Further studies and research are needed to explore the potential uses and properties of [(3R)-3-fluorooxolan-3-yl]Methanol, as its applications may extend beyond the current understanding.

Check Digit Verification of cas no

The CAS Registry Mumber 1123787-01-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,3,7,8 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1123787-01:
(9*1)+(8*1)+(7*2)+(6*3)+(5*7)+(4*8)+(3*7)+(2*0)+(1*1)=138
138 % 10 = 8
So 1123787-01-8 is a valid CAS Registry Number.

1123787-01-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3R)-3-fluorotetrahydrofuran-3-yl]methanol

1.2 Other means of identification

Product number -
Other names (R)-(3-fluorotetrahydrofuran-3-yl)methanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1123787-01-8 SDS

1123787-01-8Downstream Products

1123787-01-8Relevant articles and documents

A broadly applicable and practical oligomeric (salen)Co catalyst for enantioselective epoxide ring-opening reactions

White, David E.,Tadross, Pamela M.,Lu, Zhe,Jacobsen, Eric N.

, p. 4165 - 4180 (2014/06/09)

The (salen)Co catalyst (4a) can be prepared as a mixture of cyclic oligomers in a short, chromatography-free synthesis from inexpensive, commercially available precursors. This catalyst displays remarkable enhancements in reactivity and enantioselectivity relative to monomeric and other multimeric (salen)Co catalysts in a wide variety of enantioselective epoxide ring-opening reactions. The application of catalyst 4a is illustrated in the kinetic resolution of terminal epoxides by nucleophilic ring-opening with water, phenols, and primary alcohols; the desymmetrization of meso epoxides by addition of water and carbamates; and the desymmetrization of oxetanes by intramolecular ring opening with alcohols and phenols. The favorable solubility properties of complex 4a under the catalytic conditions facilitated mechanistic studies, allowing elucidation of the basis for the beneficial effect of oligomerization. Finally, a catalyst selection guide is provided to delineate the specific advantages of oligomeric catalyst 4a relative to (salen)Co monomer 1 for each reaction class.

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