Home Carboxys 1-Cyclohexene-1-carboxylic acid

1-Cyclohexene-1-carboxylic acid

CAS No.:
636-82-8
Catalog Number:
AG003E94
Molecular Formula:
C7H10O2
Molecular Weight:
126.1531
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$25
- +
5g
95%
In Stock USA
United States
$88
- +
25g
95%
In Stock USA
United States
$350
- +
Product Description
Catalog Number:
AG003E94
Chemical Name:
1-Cyclohexene-1-carboxylic acid
CAS Number:
636-82-8
Molecular Formula:
C7H10O2
Molecular Weight:
126.1531
MDL Number:
MFCD00001545
IUPAC Name:
cyclohexene-1-carboxylic acid
InChI:
InChI=1S/C7H10O2/c8-7(9)6-4-2-1-3-5-6/h4H,1-3,5H2,(H,8,9)
InChI Key:
NMEZJSDUZQOPFE-UHFFFAOYSA-N
SMILES:
OC(=O)C1=CCCCC1
Properties
Complexity:
147  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
126.068g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
126.155g/mol
Monoisotopic Mass:
126.068g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
1.7  
Literature
Title Journal
Naphthenic acid biodegradation by the unicellular alga Dunaliella tertiolecta. Chemosphere 20110701
Physical exercise reduces circulating lipopolysaccharide and TLR4 activation and improves insulin signaling in tissues of DIO rats. Diabetes 20110301
Biosynthesis of rapamycin and its regulation: past achievements and recent progress. The Journal of antibiotics 20100801
Factors that affect oxygen activation and coupling of the two redox cycles in the aromatization reaction catalyzed by NikD, an unusual amino acid oxidase. Biochemistry 20091013
Genomic and microarray analysis of aromatics degradation in Geobacter metallireducens and comparison to a Geobacter isolate from a contaminated field site. BMC genomics 20070101
Neuroprotective and free radical scavenging activities of phenolic compounds from Hovenia dulcis. Archives of pharmacal research 20050701
The effects of benzoate, cyclohex-1-ene carboxylate, and cyclohexane carboxylate on biotransformation of o-phthalate in sediment slurries under sulfate-reducing conditions. Chemosphere 20050301
Degradation pathways of cyclic alkanes in Rhodococcus sp. NDKK48. Applied microbiology and biotechnology 20041101
Mutasynthesis of enterocin and wailupemycin analogues. Journal of the American Chemical Society 20030806
High-performance nanocatalysts for single-step hydrogenations. Accounts of chemical research 20030101
Molecular characterization of NikD, a new flavoenzyme important in the biosynthesis of nikkomycin antibiotics. Biochemistry 20021231
Properties