79205-55-3 Usage
Uses
Used in Organic Synthesis:
(1-fluoro-cyclopentyl)-hydroxy-acetonitrile is used as an intermediate in organic synthesis for the production of various chemicals. Its unique properties, such as reactivity and solubility, make it a valuable component in the synthesis of complex organic molecules.
Used in Research:
(1-fluoro-cyclopentyl)-hydroxy-acetonitrile is used as a research compound to study its physical and chemical properties, as well as its potential applications in various fields. Researchers may investigate its reactivity, stability, and interactions with other compounds to better understand its potential uses and limitations.
Used in Industrial Processes:
(1-fluoro-cyclopentyl)-hydroxy-acetonitrile may have applications in industrial processes, where its unique properties can be utilized for specific tasks or reactions. Its potential use in the production of pharmaceuticals, agrochemicals, or other specialty chemicals could be explored, depending on its reactivity and compatibility with other compounds in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 79205-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,0 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79205-55:
(7*7)+(6*9)+(5*2)+(4*0)+(3*5)+(2*5)+(1*5)=143
143 % 10 = 3
So 79205-55-3 is a valid CAS Registry Number.
79205-55-3Relevant academic research and scientific papers
GPR119 Agonists
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Page/Page column 7-8, (2011/02/18)
GPR119 agonist compounds of the formula: and pharmaceutical compositions for the treatment of diabetes and obesity.
NOUVELLE VOIE DE SYNTHESE D'ACIDES AMINES MONOFLUORES
Ayi, A. I.,Remli, M.,Guedj, R.
, p. 1505 - 1508 (2007/10/02)
Ring opening of the glycidonitriles (IIa-e) by HF/pyridine leads to the fluorocyanohydrins (IIIa-e).Treatment of the nitriles (IIIa-e) with ammonia in methanol gives the α-amino-β-fluoro nitriles (IVa-e) which upon acidic hydrolysis afford the β-fluoro-α-
NEW SYNTHETIC ROUTES TO β-FLUORO β-PHENYLLACTIC ACID DERIVATIVES AND Β-FLUOROCYANOHYDRINS
Ayi, A. I.,Remli, M.,Condom, R.,Guedj, R.
, p. 565 - 580 (2007/10/02)
Alkyl phenyl 2,3-epoxycarboxylates from the well-known Darzens glycidic esters synthesis react under very mild conditions with pyridinium-poly-hydrogen fluoride to give corresponding 3-fluoro 3-phenyllactates in almost quantitative yields with a high regio and stereoselectivity.This method can be applied succesfully to other flycidic derivatives: glycidoamides, glycidonitriles, glycidoiminoesters...The spectrometric properties (IR, NMR) are presented.
