Molecular structure of 2-Heptenoic Acid, CAS Number: 18999-28-5
2-Heptenoic Acid (CAS 18999-28-5)
CAS Number:
18999-28-5
Molecular Weight:
128.17
Molecular Formula:
C7H12O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
2-Heptenoic acid, also known as 2-heptenoate or enanthic acid, is an organic compound with the chemical formula C7H12O2. It is a carboxylic acid characterized by a seven-carbon chain with a double bond between the second and third carbon atoms. 2-Heptenoic acid can exist as geometric isomers, namely cis-2-heptenoic acid and trans-2-heptenoic acid, depending on the orientation of the double bond.
2-Heptenoic Acid (CAS 18999-28-5) References
- Investigations on the catalytic carboxylation of olefins with CO2 towards α,β-unsaturated carboxylic acid salts: characterization of intermediates and ligands as well as substrate effects. | Jevtovikj, I., et al. 2015. Dalton Trans. 44: 11083-94. PMID: 25999232
- New cofactor supports α,β-unsaturated acid decarboxylation via 1,3-dipolar cycloaddition. | Payne, KA., et al. 2015. Nature. 522: 497-501. PMID: 26083754
- Probiotics. Antistaphylococcal and antifibrinolytic activities of omega-guanidino acids and omega-guanidinoacyl-L-histidines. | Fujii, A. and Cook, ES. 1973. J Med Chem. 16: 1409-11. PMID: 4765868
- Amino acid analogs. 2. 3-Fluoroamino acids. 1. Chain length three to seven carbon atoms. | Gershon, H. and McNeil, MW. 1973. J Med Chem. 16: 1407-9. PMID: 4797293
- Volatile compounds in oils after deep frying or stir frying and subsequent storage | Wu, C. M., & Chen, S. Y. 1992. Journal of the American Oil Chemists' Society. 69(9): 858-865.
- On-Line Derivatization for Complex Fatty Acid Mixtures by Capillary Gas Chromatography/Mass Spectrometry | Nimz, E. L., & Morgan, S. L. 1993. Journal of chromatographic science. 31(4): 145-149.
- Novel Water-Soluble Organosilane Compounds as a Radical Reducing Agent in Aqueous Media | Yamazaki, O., Togo, H., Nogami, G., & Yokoyama, M. 1997. Bulletin of the Chemical Society of Japan. 70(10): 2519-2523.
- Identification of novel malodour compounds in laundry | Takeuchi, K., Hasegawa, Y., Ishida, H., & Kashiwagi, M. 2012. Flavour and fragrance journal. 27(1): 89-94.
- Utilization of 2-alkenoic acids for biosynthesis of medium-chain-length polyhydroxyalkanoates in metabolically engineered Escherichia coli to construct a novel chemical recycling system | Sato, S., Ishii, N., Hamada, Y., Abe, H., & Tsuge, T. 2012. Polymer degradation and stability. 97(3): 329-336.
- Transition metal free large-scale synthesis of aromatic vinyl chlorides from aromatic vinyl carboxylic acids using bleach | Hatvate, N. T., Takale, B. S., Ghodse, S. M., & Telvekar, V. N. 2018. Tetrahedron Letters. 59(43): 3892-3894.
- Effects of Nitrogen and Sulfur Deprivation on β-Carotene and Fatty Acid content of Dunaliella salina | Khademi, H., Morowvat, M. H., & Ghasemi, Y. 2018. Trends in Pharmaceutical Sciences. 4(3): 187-196.
- Influence of Fe/HZSM-5 catalyst on elemental distribution and product properties during hydrothermal liquefaction of Nannochloropsis sp. | Liu, Z., Li, H., Zeng, J., Liu, M., Zhang, Y., & Liu, Z. 2018. Algal research. 35: 1-9.
- GC–MS analysis of phytoconstituents present in methanolic extract of Actinidia deliciosa L. fruits and its antioxidant activity | Qadir, A., Khan, N., Ullah, S. N. M. N., Ali, A., Gupta, D. K., & Khan, S. A. 2022. Journal of the Indian Chemical Society. 99(7): 100566.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Heptenoic Acid, 5 ml | sc-288120 | 5 ml | $354.00 |