108811-61-6 Usage
Description
4-(2-FURYL)-3-BUTEN-2-ONE 95% CIS AND& is a chemical compound that is involved in various chemical reactions, including base catalyzed aldol condensation of furfurals with acetone or propanal. It also participates in aldol-condensation and hydrogenation reactions of synthetic bio-oils at 100°C and 400 psi in a biphasic system of decalin/water.
Uses
Used in Chemical Synthesis:
4-(2-FURYL)-3-BUTEN-2-ONE 95% CIS AND& is used as a reactant in chemical synthesis for the production of various compounds. Its ability to participate in base catalyzed aldol condensation reactions makes it a valuable component in the synthesis of complex organic molecules.
Used in Bio-oil Processing:
4-(2-FURYL)-3-BUTEN-2-ONE 95% CIS AND& is used in the processing of synthetic bio-oils, where it participates in aldol-condensation and hydrogenation reactions at high temperatures and pressures. This allows for the upgrading of bio-oils and the production of valuable chemicals and materials.
Used in Pharmaceutical Industry:
4-(2-FURYL)-3-BUTEN-2-ONE 95% CIS AND& may also have potential applications in the pharmaceutical industry, as its chemical properties can be utilized in the development of new drugs and therapeutic agents. Further research and development would be required to explore these potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 108811-61-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,8,1 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108811-61:
(8*1)+(7*0)+(6*8)+(5*8)+(4*1)+(3*1)+(2*6)+(1*1)=116
116 % 10 = 6
So 108811-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O2/c1-7(9)4-5-8-3-2-6-10-8/h2-6H,1H3/b5-4+
108811-61-6Relevant articles and documents
Wittig reactions of stabilized phosphorus ylides with aldehydes in water
Wu, Jinlong,Zhang, Da,Wei, Shaoyong
, p. 1213 - 1222 (2005)
The Wittig reactions of three stabilized phosphorus ylides with aldehydes in water were investigated. Most of the olefination reactions completed within 5-60 min in refluxing water in the presence of 1.2 M LiCl to afford the olefin products in 65-98% yields. It was found that the Wittig reactions of stabilized phosphorus ylides with aldehydes in water were faster than those carried out in organic solvents. Copyright Taylor & Francis, Inc.
A highly selective synthesis of (Z)-α,β-unsaturated ketones
Yu, Wensheng,Su, Mei,Jin, Zhendong
, p. 6725 - 6728 (2007/10/03)
New Wadsworth-Emmons reagents, bis(2,2,2-trifluoroethyl)-(2-oxopropyl)phosphonate 6 and bis(2,2,2-trifluoroethyl)-(1-methyl-2-oxopropyl)-phosphonate 7 were prepared and their reactions with aldehydes yielded disubstituted and trisubstituted (Z)-α,β-unsaturated ketones.
