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2459-05-4 | 2-Butenedioic acid (2E)-, 1-ethyl ester
CAS No: 2459-05-4 Catalog No: AG002OOO MDL No:MFCD00002699
Product Description
Catalog Number:
AG002OOO
Chemical Name:
2-Butenedioic acid (2E)-, 1-ethyl ester
CAS Number:
2459-05-4
Molecular Formula:
C6H8O4
Molecular Weight:
144.1253
MDL Number:
MFCD00002699
IUPAC Name:
(E)-4-ethoxy-4-oxobut-2-enoic acid
InChI:
InChI=1S/C6H8O4/c1-2-10-6(9)4-3-5(7)8/h3-4H,2H2,1H3,(H,7,8)/b4-3+
InChI Key:
XLYMOEINVGRTEX-ONEGZZNKSA-N
SMILES:
CCOC(=O)/C=C/C(=O)O
UNII:
Y3W849NG2N
NSC Number:
244252
Properties
Complexity:
159
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Exact Mass:
144.042g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
144.126g/mol
Monoisotopic Mass:
144.042g/mol
Rotatable Bond Count:
4
Topological Polar Surface Area:
63.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2
Literature
| Title | Journal |
|---|---|
| Photo-crosslinked networks prepared from fumaric acid monoethyl ester-functionalized poly(D,L-lactic acid) oligomers and N-vinyl-2-pyrrolidone for the controlled and sustained release of proteins. | Acta biomaterialia 20121001 |
| Photo-crosslinked biodegradable hydrogels prepared from fumaric acid monoethyl ester-functionalized oligomers for protein delivery. | Macromolecular bioscience 20120501 |
| Structure-activity relationships of trans-substituted-propenoic acid derivatives on the nicotinic acid receptor HCA2 (GPR109A). | Bioorganic & medicinal chemistry letters 20110501 |
| Treatment of recurrent aphthous stomatitis with fumaric acid esters. | Archives of dermatology 20110301 |
| Rapid photo-crosslinking of fumaric acid monoethyl ester-functionalized poly(trimethylene carbonate) oligomers for drug delivery applications. | Journal of controlled release : official journal of the Controlled Release Society 20101001 |
| Creep-resistant elastomeric networks prepared by photocrosslinking fumaric acid monoethyl ester-functionalized poly(trimethylene carbonate) oligomers. | Acta biomaterialia 20090601 |
| Fumaric acid monoethyl ester-functionalized poly(D,L-lactide)/N-vinyl-2-pyrrolidone resins for the preparation of tissue engineering scaffolds by stereolithography. | Biomacromolecules 20090209 |
| Fumaric acid esters in necrobiosis lipoidica: results of a prospective noncontrolled study. | The British journal of dermatology 20051001 |
| Preparation of biodegradable networks by photo-crosslinking lactide, epsilon-caprolactone and trimethylene carbonate-based oligomers functionalized with fumaric acid monoethyl ester. | Biomaterials 20050601 |
| Preparation of hydrogels by photo-crosslinking of fumaric acid monoethyl ester (fame) functionalized oligomers. | Journal of controlled release : official journal of the Controlled Release Society 20050103 |
| In vitro pharmacokinetics of anti-psoriatic fumaric acid esters. | BMC pharmacology 20040101 |
| Presystemic metabolism and intestinal absorption of antipsoriatic fumaric acid esters. | Biopharmaceutics & drug disposition 20030901 |
| Treatment of disseminated granuloma annulare with fumaric acid esters. | BMC dermatology 20020101 |
| Successful treatment of recalcitrant cutaneous sarcoidosis with fumaric acid esters. | BMC dermatology 20020101 |
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