4415-82-1 Usage
Description
Cyclobutanemethanol, a colorless to almost colorless clear liquid, is a chemical compound that has been investigated for its oxidation properties in the presence of lead tetraacetate and lead tetraacetate/metal chloride. It is also a drug used to treat inflammatory diseases and has shown potential in the synthesis of bicyclic lactone.
Uses
Used in Pharmaceutical Industry:
Cyclobutanemethanol is used as an anti-inflammatory agent for its ability to inhibit the CB2 receptor, which is prevalent in inflammatory tissues. This application helps in reducing inflammation and managing inflammatory diseases.
Used in Drug Synthesis:
Cyclobutanemethanol is used as a key compound in the synthesis of bicyclic lactone, which has potential applications in the development of new drugs.
Used in Antiviral Applications:
Cyclobutanemethanol has demonstrated its potential as an antiviral agent by inhibiting influenza virus replication in vitro. This suggests that it could be used in the development of antiviral medications.
Used in Inflammatory Disease Treatment:
Cyclobutanemethanol is used as an uptake inhibitor, blocking the transport of uridine into cells and preventing the activation of G-protein coupled receptors. This action leads to the suppression of inflammatory mediator production, making it a valuable component in the treatment of inflammatory diseases.
Used in Enhancing Blood Flow:
Cyclobutanemethanol acts on vascular endothelial cells, increasing blood flow to inflamed areas and providing relief from inflammation-related discomfort.
Used in Preventing Dehydration:
Cyclobutanemethanol has been shown to prevent dehydration, which can be beneficial in maintaining the body's fluid balance and overall health.
Synthesis
Cyclobutanemethanol can be synthesized from two molecules of hydrochloric acid and one molecule of cyclobutane. The synthesis pathway includes removal of a hydroxy group and addition of an alkynyl group via hydrogen bonding interactions with chloride ions.
Check Digit Verification of cas no
The CAS Registry Mumber 4415-82-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4415-82:
(6*4)+(5*4)+(4*1)+(3*5)+(2*8)+(1*2)=81
81 % 10 = 1
So 4415-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O/c6-4-5-2-1-3-5/h5-6H,1-4H2
4415-82-1Relevant articles and documents
Cobalt Pincer Complexes for Catalytic Reduction of Carboxylic Acid Esters
Junge, Kathrin,Wendt, Bianca,Cingolani, Andrea,Spannenberg, Anke,Wei, Zhihong,Jiao, Haijun,Beller, Matthias
supporting information, p. 1046 - 1052 (2018/01/01)
A selection of cobalt(I) and cobalt(II) pincer type complexes with different substitution patterns was tested in the catalytic reduction of carboxylic acid esters to alcohols. The cobalt pincer type complex 4 is suitable for the hydrogenation of aromatic as well as aliphatic and cyclic esters. Mechanistic investigation indicated a metal ligand cooperated reaction pathway.
Synthesis method of analgesic intermediate bromomethyl cyclobutane
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Paragraph 0009; 0010; 0011; 0012; 0013; 0014, (2017/07/21)
The invention relates to a synthesis method of analgesic intermediate bromomethyl cyclobutane. The synthesis method comprises the following steps: by taking ethylene and acrylic acid as starting materials, carrying out Diels-Alder reaction to obtain cyclobutanecarboxylic acid, then reducing to obtain cyclobutanemethanol, and then brominating to obtain high-purity bromomethyl cyclobutane, wherein the total yield reaches more than 65%. The synthesis method provided by the invention has the advantages of available raw materials, mild reaction conditions, simple postprocessing operation, small environmental pollution, short reaction time, high reaction operational safety, high reaction yield, good product quality and low cost, and industrial production is facilitated.