
Identification
CAS Number
849762-24-9
Name
BLATTELLAQUINONE CAS 849762-24-9
Synonyms
849762-24-9
Blattellaquinone
gentisyl quinone isovalerate
DTXSID00464047
V44AK4849M
(3,6-Dioxo-1,4-cyclohexadien-1-yl)methyl 3-methylbutanoate
RefChem:905924
DTXCID60414866
(3,6-Dioxocyclohexa-1,4-dien-1-yl)methyl 3-methylbutanoate
MFCD08752330
(3,6-dioxocyclohexa-1,4-dienyl)methyl 3-methylbutanoate
Gentisylquinone isovalerate
(3,6-Dioxocyclohexa-1,4-dien-1-yl)methyl 3-Methylbutanoate ; Gentisylquinone Isovalerate ;
Butanoic acid, 3-methyl-, (3,6-dioxo-1,4-cyclohexadien-1-yl)methyl ester
BUTANOICACID, 3-METHYL-, (3,6-DIOXO-1,4-CYCLOHEXADIEN-1-YL)METHYL ESTER
SMILES
CC(C)CC(=O)OCC1=CC(=O)C=CC1=O
StdInChI
InChI=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
StdInChIKey
JVMUMZYOAWLJQW-UHFFFAOYSA-N
Molecular Formula
C12H14O4
Molecular Weight
222.24
Properties
Appearance
Yellow solid powder
Safety Data
Symbol
Signal Word
Warning
Hazard statements
H302, H315, H319, H335Precautionary Statements
P260, P271, P501, P101, P280, P301+P310, P304+P340, P305+P351+P338, P303+P361+P353, P405, P301+P330+P331, P403+P233, P321Specifications and Other Information of Our BLATTELLAQUINONE CAS 849762-24-9
Identification Methods
HNMR, HPLC
Purity
98% min
Max single impurity
≤2%
Shelf Life
2 years
Storage
Store below 5° for a long time, sealed and away from light
Known Application
1. 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 2. 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 3. 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 4. 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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