200,000+ products from a single source!
sales@angenechem.com
Home > Other Building Blocks > 121652-00-4
121652-00-4 | 2-Cyclohexen-1-one, 4-hydroxy-, (4S)-
CAS No: 121652-00-4 Catalog No: AG0015HY MDL No:
Product Description
Catalog Number:
AG0015HY
Chemical Name:
2-Cyclohexen-1-one, 4-hydroxy-, (4S)-
CAS Number:
121652-00-4
Molecular Formula:
C6H8O2
Molecular Weight:
112.1265
IUPAC Name:
4-hydroxycyclohex-2-en-1-one
InChI:
InChI=1S/C6H8O2/c7-5-1-2-6(8)4-3-5/h1-2,5,7H,3-4H2
InChI Key:
AMFCFGFZMSQOIU-UHFFFAOYSA-N
SMILES:
O[C@H]1CCC(=O)C=C1
Properties
Complexity:
127
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
112.052g/mol
Formal Charge:
0
Heavy Atom Count:
8
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
112.128g/mol
Monoisotopic Mass:
112.052g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.2
Literature
| Title | Journal |
|---|---|
| Fabrication of magnetic chitosan nanoparticles grafted with β-cyclodextrin as effective adsorbents toward hydroquinol. | Colloids and surfaces. B, Biointerfaces 20120615 |
| The ascorbate-glutathione-α-tocopherol triad in abiotic stress response. | International journal of molecular sciences 20120101 |
| Neutral histidine and photoinduced electron transfer in DNA photolyases. | Journal of the American Chemical Society 20111116 |
| Degradation of pentachlorophenol and 2,4-dichlorophenol by sequential visible-light driven photocatalysis and laccase catalysis. | Environmental science & technology 20101201 |
| The thio-adduct facilitated, enzymatic kinetic resolution of 4-hydroxycyclopentenone and 4-hydroxycyclohexenone. | Organic & biomolecular chemistry 20100207 |
| Concise synthesis of an antifeedant sesquiterpene against Locusta migratoria. | Bioscience, biotechnology, and biochemistry 20100101 |
| An efficient protocol for the enantioselective preparation of a key polyfunctionalized cyclohexane. New access to (R)- and (S)-4-Hydroxy-2-cyclohexenone and (R)- and (S)-trans-cyclohex-2-ene-1,4-diol. | The Journal of organic chemistry 20080502 |
| Degradation of 4-fluorophenol by Arthrobacter sp. strain IF1. | Applied microbiology and biotechnology 20080301 |
| Chlorobenzene degradation by electro-heterogeneous catalysis in aqueous solution: intermediates and reaction mechanism. | Journal of environmental sciences (China) 20080101 |
| A new competitive enzyme-linked immunosorbent assay (ELISA) for determination of estrogenic bisphenols. | Talanta 20020719 |
| A new and efficient chemoenzymatic route to both enantiomers of 4-hydroxycyclohex-2-en-1-one. | Organic letters 20020613 |
Related Products
Featured Products
© 2019 Angene International Limited. All rights Reserved.