1. Home
  2. 2-Propenoic acid, 2-cyano-3-(2-furanyl)-, ethyl ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Propenoic acid, 2-cyano-3-(2-furanyl)-, ethyl ester

CCOC(=O)/C(=C/c1ccco1)/C#N Request for Quotation
Chemical Name: 2-Propenoic acid, 2-cyano-3-(2-furanyl)-, ethyl ester
CAS Number: 23973-22-0
Product Number: AG003Q3W(AGN-PC-0JNBKP)
Synonyms:
MDL No: MFCD00137603
Molecular Formula: C10H9NO3
Molecular Weight: 191.1834

Identification/Properties

Computed Properties
Molecular Weight:
191.186g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
191.058g/mol
Monoisotopic Mass:
191.058g/mol
Topological Polar Surface Area:
63.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
287
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
1
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The application of Ethyl 2-Cyano-3-(2-furanyl)acrylate in chemical synthesis is particularly noteworthy in organic chemistry. This compound serves as a versatile building block for the synthesis of a variety of complex organic molecules due to its unique structural properties. Ethyl 2-Cyano-3-(2-furanyl)acrylate is commonly employed in the preparation of heterocyclic compounds and pharmaceutical agents. Its cyano and furan groups enable diverse reactivity, allowing for the introduction of functional groups and the formation of new carbon-carbon and carbon-heteroatom bonds. Furthermore, this compound can undergo numerous synthetically useful transformations, such as addition reactions, cyclizations, and further derivatizations, making it a valuable tool for organic chemists in the design and synthesis of novel compounds with potential biological activities.