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Home Other Building Blocks 2-Pentynoic acid

2-Pentynoic acid

CAS No.:
5963-77-9
Catalog Number:
AG003HUA
Molecular Formula:
C5H6O2
Molecular Weight:
98.0999
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$47
- +
5g
95%
In Stock USA
United States
$182
- +
25g
95%
In Stock USA
United States
$725
- +
Product Description
Catalog Number:
AG003HUA
Chemical Name:
2-Pentynoic acid
CAS Number:
5963-77-9
Molecular Formula:
C5H6O2
Molecular Weight:
98.0999
MDL Number:
MFCD05864027
IUPAC Name:
pent-2-ynoic acid
InChI:
InChI=1S/C5H6O2/c1-2-3-4-5(6)7/h2H2,1H3,(H,6,7)
InChI Key:
MINRDQDGBLQBGD-UHFFFAOYSA-N
SMILES:
CCC#CC(=O)O
NSC Number:
289567
Properties
Complexity:
124  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
98.037g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
98.101g/mol
Monoisotopic Mass:
98.037g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2  
Literature
Title Journal
Automated determination of total captopril in urine by liquid chromatography with post-column derivatization coupled to on-line solid phase extraction in a sequential injection manifold. Talanta 20120115
High throughput automated determination of glutathione based on the formation of a UV-absorbing thioacrylate derivative. Combinatorial chemistry & high throughput screening 20100701
Ethyl-propiolate as a novel and promising analytical reagent for the derivatization of thiols: study of the reaction under flow conditions. Journal of pharmaceutical and biomedical analysis 20091015
Synthesis of hydroxycoumarins and hydroxybenzo[f]- or [h]coumarins as lipid peroxidation inhibitors. Bioorganic & medicinal chemistry letters 20090215
Synthesis of molecular brushes by 'grafting onto' method: combination of ATRP and click reactions. Journal of the American Chemical Society 20070523
Properties