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10248-82-5 | 1-Penten-1-one
CAS No: 10248-82-5 Catalog No: AG0007KB MDL No:
Product Description
Catalog Number:
AG0007KB
Chemical Name:
1-Penten-1-one
CAS Number:
10248-82-5
Molecular Formula:
C5H8O
Molecular Weight:
84.1164
IUPAC Name:
pent-1-en-1-one
InChI:
InChI=1S/C5H8O/c1-2-3-4-5-6/h4H,2-3H2,1H3
InChI Key:
CSIJVUYEABVULE-UHFFFAOYSA-N
SMILES:
CCCC=C=O
Properties
Complexity:
60.3
Compound Is Canonicalized:
No
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
84.058g/mol
Formal Charge:
0
Heavy Atom Count:
6
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
84.118g/mol
Monoisotopic Mass:
84.058g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1
Literature
| Title | Journal |
|---|---|
| Synthesis and structure-activity relationships of varied ether linker analogues of the antitubercular drug (6S)-2-nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5h-imidazo[2,1-b][1,3]oxazine (PA-824). | Journal of medicinal chemistry 20111013 |
| Protein glycoengineering enabled by the versatile synthesis of aminooxy glycans and the genetically encoded aldehyde tag. | Journal of the American Chemical Society 20111012 |
| Coupling carbohydrates to proteins for glycoconjugate vaccine development using a pentenoyl group as a convenient linker. | Methods in molecular biology (Clifton, N.J.) 20110101 |
| Enhancement of the click chemistry for the inverse Diels Alder technology by functionalization of amide-based monomers. | International journal of medical sciences 20110101 |
| Modification, crosslinking and reactive electrospinning of a thermoplastic medical polyurethane for vascular graft applications. | Acta biomaterialia 20100701 |
| A palladium(II)-catalyzed synthesis of spiroacetals through a one-pot multicomponent cascade reaction. | Angewandte Chemie (International ed. in English) 20090101 |
| Desymmetrization of 7-azabicycloalkenes by tandem olefin metathesis for the preparation of natural product scaffolds. | Beilstein journal of organic chemistry 20070101 |
| The N-pentenoyl protecting group for aminoacyl-tRNAs. | Methods (San Diego, Calif.) 20050701 |
| An efficient chemoenzymatic approach to (S)-gamma-fluoroleucine ethyl ester. | The Journal of organic chemistry 20050318 |
| Synthesis and immunological properties of N-modified GM3 antigens as therapeutic cancer vaccines. | Journal of medicinal chemistry 20050210 |
| Variation of major volatile constituents in various green teas from Southeast Asia. | Journal of agricultural and food chemistry 20010301 |
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