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(R)-4-hydroxy-5-methylfuran-2(5H)-one
  • Chemical Name: (R)-4-hydroxy-5-methylfuran-2(5H)-one
  • CAS No.: 22885-98-9

Buy cost-effective 99% pure (R)-4-hydroxy-5-methylfuran-2(5H)-one 22885-98-9 now

  • Molecular Formula: C5H6 O3
  • Molecular Weight: 114.101
  • Vapor Pressure: 0.0411mmHg at 25°C 
  • Melting Point: 115°C 
  • Refractive Index: 1.4056 (estimate) 
  • Boiling Point: 211.5°Cat760mmHg 
  • Flash Point: 93.9°C 
  • PSA: 46.53000 
  • Density: 1.349g/cm3 
  • LogP: 0.37360 

(R)-4-hydroxy-5-methylfuran-2(5H)-one(Cas 22885-98-9) Usage

General Description

(R)-4-hydroxy-5-methylfuran-2(5H)-one, also known as carnosic acid, is a naturally occurring organic compound found in rosemary and other herbs. It is a potent antioxidant and has been shown to have anti-inflammatory, anti-cancer, and neuroprotective properties. Carnosic acid is often used in food and cosmetic products due to its ability to extend shelf life and protect against oxidation. It also has potential applications in the pharmaceutical industry for the treatment of various diseases. The compound's unique chemical structure and diverse range of biological activities make it a valuable subject of research for potential therapeutic and industrial uses.

InChI:InChI=1/C5H6O3/c1-3-4(6)2-5(7)8-3/h2-3,7H,1H3

22885-98-9 Relevant articles

A Short Synthesis of the Mould Metabolite (R)-(+)-Carolinic Acid from (S)-Lactic Acid

Linder, David,Schobert, Rainer

, p. 4564 - 4568 (2016/12/14)

(R)-(+)-Carolinic acid was prepared in s...

Baker's Yeast Mediated Bioreduction of Prochiral Ketones Having 6-(4-Oxo-1,3-dioxinyl) Group

Sakaki, Jun-ichi,Suzuki, Miwako,Kobayashi, Satoshi,Sato, Masayuki,Kaneko, Chikara

, p. 901 - 904 (2007/10/02)

Prochiral ketones having 6-(4-oxo-1,3-di...

22885-98-9 Process route

(R)-4-benzyloxy-5-methylfuran-2(5H)-one

(R)-4-benzyloxy-5-methylfuran-2(5H)-one

(R)-4-hydroxy-5-methylfuran-2(5H)-one
22885-98-9

(R)-4-hydroxy-5-methylfuran-2(5H)-one

(R)-5-methyltetronic acid
5457-19-2

(R)-5-methyltetronic acid

Conditions
Conditions Yield
With 5%-palladium/activated carbon; hydrogen; In methanol; at 20 ℃; for 1.5h; under 750.075 Torr; Overall yield = 99 %; Overall yield = 1.12 g;
6-(1-Hydroxyethyl)-2,2-dimethyl-1,3-dioxin-4-one
128766-64-3

6-(1-Hydroxyethyl)-2,2-dimethyl-1,3-dioxin-4-one

(R)-4-hydroxy-5-methylfuran-2(5H)-one
22885-98-9

(R)-4-hydroxy-5-methylfuran-2(5H)-one

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: PCC
2: 1.) fermenting baker's yeast, 32 deg C, 1 d 2.) toluene, reflux
With pyridinium chlorochromate;

22885-98-9 Upstream products

  • 130473-32-4
    130473-32-4

    6-Acetyl-2,2-dimethyl-1,3-dioxin-4-one

  • 128766-64-3
    128766-64-3

    6-(1-Hydroxyethyl)-2,2-dimethyl-1,3-dioxin-4-one