BLATTELLAQUINONE CAS#: 849762-24-9; ChemWhat Code: 1247136

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NameBLATTELLAQUINONE
IUPAC Name(3,6-dioxocyclohexa-1,4-dien-1-yl)methyl 3-methylbutanoate
Molecular Structure(3,6-dioxocyclohexa-1,4-dien-1-yl)methyl 3-methylbutanoate
CAS Registry Number 849762-24-9
EINECS NumberNo data available
MDL NumberNo data available
Beilstein Registry NumberNo data available
Synonymsblattellaquinonegentisyl quinone isovalerate
Molecular FormulaC12H14O4
Molecular Weight222.24
InChIInChI=1S/C12H14O4/c1-8(2)5-12(15)16-7-9-6-10(13)3-4-11(9)14/h3-4,6,8H,5,7H2,1-2H3
InChI KeyJVMUMZYOAWLJQW-UHFFFAOYSA-N
Canonical SMILESCC(C)CC(=O)OCC1=CC(=O)C=CC1=O
Patent Information
Patent IDTitlePublication Date
WO2006/19648GERMAN COCKROACH ATTRACTANT2006

Physical Data

AppearanceYellow solid powder
SolubilitySoluble in chloroform (a small amount) and methanol (a small amount)
Flash PointNo data available
Refractive indexNo data available
SensitivityNo data available
Melting Point, °C Solvent (Melting Point)
46 – 47hexane

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)Frequency (NMR Spectroscopy), MHz
Chemical shifts1Hchloroform-d1300
Chemical shifts13Cchloroform-d175
1H600
BLATTELLAQUINONE CAS#: 849762-24-9 NMRHNMR of BLATTELLAQUINONE CAS 849762-24-9
Description (IR Spectroscopy)Solvent (IR Spectroscopy)
Bandspotassium bromide
Description (Mass Spectrometry)Comment (Mass Spectrometry)
EI (Electron impact), HRMS (High resolution mass spectrometry), Spectrum
EI (Electron impact)mol peak
HRMS (High resolution mass spectrometry), EI (Electron impact)mol peak
EI (Electron impact), GCMS (Gas chromatography mass spectrometry)
CI (Chemical ionization), GCMS (Gas chromatography mass spectrometry)

Route of Synthesis (ROS)

Route of Synthesis (ROS) of BLATTELLAQUINONE CAS 849762-24-9
Route of Synthesis (ROS) of BLATTELLAQUINONE CAS 849762-24-9
ConditionsYield
With Oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 1h;98%
With oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 1h;98%
With ammonium cerium(IV) nitrate In water; acetonitrile at 20℃; for 0.5h;

Safety and Hazards

GHS Hazard StatementsNot Classified

Other Data

TransportationNONH for all modes of transport
Under the room temperature and away from light
HS CodeNo data available
StorageUnder the room temperature and away from light
Shelf Life2 years
Market PriceUSD
Druglikeness
Lipinski rules component
Molecular Weight222.241
logP0.986
HBA4
HBD0
Matching Lipinski Rules4
Veber rules component
Polar Surface Area (PSA)60.44
Rotatable Bond (RotB)5
Matching Veber Rules2
Use Pattern
german cockroach (Blattella germanica); synthetic pheromone of
Natural Product and Biological Activity Research First isolated from cockroach extracts, blattaquinone was named blattaquinone. Research has shown it to possess certain antibacterial, antifungal, and insect pheromone activities. Common Applications: Insect Chemical Ecology Research (Studying cockroach odor and signaling mechanisms); Natural Product Structure and Metabolic Pathway Research
Chemical Ecology and Behavior Research It acts as a warning or sex pheromone in insects and is therefore used in: Basic research on the development of insect attractants or behavior modulators; Research on model compounds for ecological repellents
Medicinal Chemistry and Chemical Biology Research Due to the reversible redox properties of its benzoquinone structure, it is used in the screening of drug lead compounds: Antimicrobial, antitumor, and antioxidant research models; Research on enzyme inhibitors or signaling molecules
Organic Synthesis Intermediate The quinone ester structure can be used as an intermediate in the synthesis of more complex quinone, naphthoquinone, or isophenone compounds; and as a raw material for the development of dyes, photosensitive materials, or polymerization initiators in fine chemicals (research phase).

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