294857-29-7 Usage
General Description
2,4-Furandimethanol is a biobased chemical that is derived from renewable sources such as biomass or agricultural waste. It is a versatile compound that can be used in a variety of industrial applications, including as a building block for the production of polymers, resins, and plastics. 2,4-Furandimethanol is popular due to its high performance, low toxicity, and environmental friendliness. It can be converted into a wide range of derivatives, making it a promising candidate for the development of sustainable and eco-friendly materials. Additionally, it has potential applications in the production of biofuels and as a platform chemical for the synthesis of other valuable compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 294857-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,8,5 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 294857-29:
(8*2)+(7*9)+(6*4)+(5*8)+(4*5)+(3*7)+(2*2)+(1*9)=197
197 % 10 = 7
So 294857-29-7 is a valid CAS Registry Number.
294857-29-7Relevant articles and documents
Reaction of isomeric (alkoxymethyl)(chloromethyl)-and bis(chloromethyl)furans with sodium diethyl phosphite
Pevzner,Ignat'ev,Ionin
, p. 25 - 36 (2007/10/03)
Reduction of alkyl (alkoxymethyl)furancarboxylates with lithium aluminum hydride leads to (alkoxymethyl)(hydroxymethyl)furans, while the reaction with structurally related acetoxymethyl derivatives yields bis(hydroxymethyl)furans. Treatment of the latter with thionyl chloride in ether in the presence of pyridine in the cold gives corresponding chloromethyl-or bis(chloromethyl)furans. These products react with sodium dialkyl phosphite under conditions of the Michaelis-Becker reaction to form mono-or diphosphonates, respectively. The yield of phosphorylated compounds is determined mainly by thermal stability of the substrate. In the case of 2,4-bis(chloromethyl)furan, nucleophilic substitution competes with halophilic attack on the chloromethyl group in the 4 position of the furan ring. As a result, a 2:1 mixture of 2-and 2,4-phosphorylated products is formed.
