60410-17-5

Basic information

• Product Name: (1R,3R)-Cyclopent-4-ene-1,3-diol Monoacetate
• Synonyms: (1R,3R)-Cyclopent-4-ene-1,3-diol Monoacetate;(1R,4R)-4-hydroxycyclopent-2-en-1-yl acetate;(1R,4R)-4-hydroxycyclopent-2-en-2-yl acetate;(1R,4R)-4-hydroxycyclopent-2-en-3-yl acetate
• CAS NO: 60410-17-5
• Molecular Formula: C₇H₁₀O₃
• Molecular Weight: 142.1525
• Mol File: 60410-17-5.mol

Chemical Properties

• Boiling Point: 208.0±40.0 °C(Predicted)
• Appearance: /
• Density: 1.17±0.1 g/cm3(Predicted)
• PKA: 14.11±0.40(Predicted)
• CAS DataBase Reference: (1R,3R)-Cyclopent-4-ene-1,3-diol Monoacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,3R)-Cyclopent-4-ene-1,3-diol Monoacetate(60410-17-5)
• EPA Substance Registry System: (1R,3R)-Cyclopent-4-ene-1,3-diol Monoacetate(60410-17-5)

Safety Data

• Hazardous Substances Data: 60410-17-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(1R,3R)-Cyclopent-4-ene-1,3-diol Monoacetate is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity allow for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, (1R,3R)-Cyclopent-4-ene-1,3-diol Monoacetate is employed as a reagent in the development of novel agrochemicals. Its role in the synthesis process contributes to the production of effective compounds for agricultural use, such as pesticides and herbicides.
Used in Organic Synthesis:
(1R,3R)-Cyclopent-4-ene-1,3-diol Monoacetate is used as a versatile reagent in organic synthesis for the preparation of a diverse array of organic compounds. Its cyclic structure and functional groups facilitate multiple synthetic pathways, making it an indispensable tool in the synthesis of complex organic molecules.

Upstream product

• 108-24-7 acetic anhydride 
• 108-05-4 vinyl acetate 
• 29783-26-4 cis-4-cyclopentene-1,3-diol 
• 54664-61-8 3,5-Diacetoxycyclopentene 

Downstream Products

• 59995-48-1 (R)-4-acetoxycyclopent-2-en-1-one 
• 1605291-77-7 C₁₅H₁₈O₄ 
• 54664-61-8 cis-1,4-diacetoxy-2-cyclopentene 

Relevant articles and documents

LIPASE-CATALYZED IRREVERSIBLE TRANSESTERIFICATION USING ENOL ESTERS: XAD-8 IMMOBILIZED LIPOPROTEIN LIPASE-CATALYZED RESOLUTION OF SECONDARY ALCOHOLS

Procedures for preparation of XAD-8 immobilized lipoprotein lipase and the resolution of secondary alcohols of synthetic value in organic solvents using this immobilized enzyme have been developed.

A Novel Asymmetric Synthesis of Chiral Cyclopentanoid Building Blocks by the Use of Chiral Lithium Amide

Enantioselective deprotonation of meso-epoxides, derived from 3-cyclopenten-1-ol, was examined using chiral lithium amide.Chiral cis-4-t-butyldimethylsiloxy-2-cyclopenten-1-ol, cis-4-tetrahydropyranyloxy-2-cyclopenten-1-ol, and their trans-isomers, which are useful chiral building blocks for the synthesis of cyclopentanoid natural compounds, were obtained with high enantiomeric excesses (72 - 90 percent ee).Both (R)- and (S)-4-hydroxy-2-cyclopenten-1-one were derived from (1S,4R)-4-t-butyldimethylsiloxy)-2-cyclopenten-1-ol stereospecifically.