20005-32-7 Usage
Uses
Tetrahydro-2-furanacetaldehyde is used as a reagent in the preparation of stereospecific compounds for the following reasons:
1. Used in Chemical Synthesis:
Tetrahydro-2-furanacetaldehyde is used as a key intermediate in the synthesis of various organic compounds, particularly those containing a tetrahydrofuran ring. Its unique structure allows for selective reactions and the formation of specific stereoisomers, which are crucial in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, Tetrahydro-2-furanacetaldehyde is used as a building block for the development of novel drugs with specific biological activities. Its ability to form stereospecific compounds makes it an essential component in the design and synthesis of targeted therapeutic agents.
3. Used in Flavor and Fragrance Industry:
Tetrahydro-2-furanacetaldehyde is also utilized in the flavor and fragrance industry to create unique scents and flavors. Its chemical properties allow for the creation of complex and nuanced aromas that can be used in a variety of consumer products, such as perfumes, candles, and food additives.
4. Used in Material Science:
In the field of material science, Tetrahydro-2-furanacetaldehyde can be used to develop new polymers and materials with specific properties. Its incorporation into polymer structures can lead to the creation of materials with enhanced mechanical, thermal, or electrical properties, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 20005-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,0 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20005-32:
(7*2)+(6*0)+(5*0)+(4*0)+(3*5)+(2*3)+(1*2)=37
37 % 10 = 7
So 20005-32-7 is a valid CAS Registry Number.
20005-32-7Relevant academic research and scientific papers
Obtention d'aldehydes γ-fonctionnels au cours de la thermolyse du percarbonate de O,O-t-butyle et O-vinyle en solution
Filliatre, Claude,Villenave, Jean-Jacques,Jaouhari, Rabih,Baratchart, Michel
, p. 352 - 356 (2007/10/02)
Owing to its peroxyester group, O,O-tert-butyl and O-vinyle peroxycarbonate may act as a free radical initiator in solution, but also, due to the presence of the vinylic insaturation, as a substrate for free radical addition reactions. - In such solvents as cumene which give free radicals unable to add to the double bond, the peroxycarbonate merely behaves as a vinyloxy radicals generator.It is thus possible to observe these radicals reacting either as formylmethyl radicals or as acetyl radicals. - In solvents such as cyclohexane which give free radicals able to add to the double bond, the reaction results in the substitution of formylmethyl groups to labile hydrogens of the solvent. - By applying the reaction to such compounds as ketones, ethers, acids and their derivatives, we could obtain γ-functional aldehydes (γ-ketoaldehydes, γ-oxaaldehydes and derivatives of succinaldehydic acids).These products are often difficult to prepare by other routes and until now only some of them have been described.
