23074-10-4 Usage
Description
5-Ethyl-2-furaldehyde is an organic compound with the chemical formula C6H6O2. It is a derivative of 2-furaldehyde, which is a heterocyclic aromatic compound with a five-membered ring containing four carbon atoms and one oxygen atom. The presence of an ethyl group attached to the 5-position of the furan ring distinguishes 5-ethyl-2-furaldehyde from other furan derivatives. 5-ETHYL-2-FURALDEHYDE is known for its unique chemical properties and potential applications in various industries.
Uses
Used in Chemical Synthesis:
5-Ethyl-2-furaldehyde is used as a key intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique structure and reactivity make it a valuable building block for the development of new molecules with potential applications in different fields.
Used in Pharmaceutical Industry:
5-Ethyl-2-furaldehyde is used as a starting material for the synthesis of N-(tert-butoxycarbonyl)-3-(benzoxazol-5-yl)alanine methyl ester derivatives. These derivatives have potential applications in the pharmaceutical industry, as they may exhibit biological activities and therapeutic properties. The synthesis of such derivatives can lead to the discovery of new drugs and treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 23074-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,7 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23074-10:
(7*2)+(6*3)+(5*0)+(4*7)+(3*4)+(2*1)+(1*0)=74
74 % 10 = 4
So 23074-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O2/c1-2-6-3-4-7(5-8)9-6/h3-5H,2H2,1H3
23074-10-4Relevant articles and documents
Synthesis of 2-substituted furanonaphthoquinones using directed metalation and cross coupling reactions
Starling, Sergia M.,Raslan, Delio S.,De Oliveira, Alaide B.
, p. 1013 - 1030 (2007/10/03)
A synthetic method for the preparation of C-2 substituted furanonaphthoquinones from ortholithium-benzamide and the 2-furan- carboxaldehyde derivative is described. Four 2-alkyl-furanonaphthoquinones and the 2-phenyl-substituted were prepared via phathalide. This route has been shown to be general application to the synthesis of furanonaphthoquinones.
A Concise Asymmetric Synthesis of the Seco Acid of Erythronolide B
Martin, Stephen F.,Pacofsky, Gregory J.,Gist, Ricky P.,Lee, Wen-Cherng
, p. 7634 - 7636 (2007/10/02)
-
THE SYNTHESIS OF 2,5-DISUBSTITUTED FURANS
Ager, David J.
, p. 5441 - 5444 (2007/10/02)
The dianion derived from the oxime of furfuraldehyde (1) reacts with electrophiles at the 5-position of the furan ring; subsequent hydrolysis of the oxime provides a useful method for the synthesis of 2,5-disubstituted furans.