N-ACETYL-4-BENZOQUINONE IMINE ,50700-49-7 _ChemCD

N-ACETYL-4-BENZOQUINONE IMINE

basic_info
Product_Name：	N-ACETYL-4-BENZOQUINONE IMINE
CAS：	50700-49-7
EnglishSynonyms：	N-ACETYL-1,4-BENZOQUINONE IMINE ; 4-(ACETYLIMINO)-2,5-CYCLOHEXADIEN-1-ONE ; N-ACETYLBENZOQUINONEIMINE ; N-(4-OXOCYCLOHEXA-2,5-DIEN-1-YLIDENE)ACETAMIDE ; ACETIMIDOQUINONE ; N-ACETYL-4-BENZOQUINONE IMINE ; N-ACETYL-P-BENZOQUINONIMINE ; N-(4-OXO-1-CYCLOHEXA-2,5-DIENYLIDENE)ACETAMIDE ; NAPQI ; N-ACETYL-P-BENZO-QUINONEIMINE ; N-(4-OXO-2,5-CYCLOHEXADIEN-1-YLIDENE)ACETAMIDE
pro_mdlNumber：	MFCD00078909
pro_acceptors：	3
pro_donors：	0
pro_smile：	CC(=O)N=C1C=CC(=O)C=C1
InChi：	InChI=1S/C8H7NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5H,1H3
InChiKey：	InChIKey=URNSECGXFRDEDC-UHFFFAOYSA-N
property
Comments：	APPLICATION: REACTANT INVOLVED IN: REDOX REACTIONS. HYDROHALOGENATION. PH DEPENDENT REACTIONS: IN ACIDIC MEDIA IT IS HYDROLYZED, HYDROXYLATED IN ALKALINE MEDIA, AND DIMERIZED AT INTERMEDIATE PHS. MEDIATION OF ACETAMINOPHEN HEPATOTOXICITY. STUDIES TO IDENTIFY THE UTILITY OF ACETAMINOPHEN FOR TREATING AUTOIMMUNE DISORDERS OTHER NOTES: ACETAMINOPHEN METABOLITE THAT REACTS WITH SERUM PROTEINS OTHER NOTES: TANDEM MASS SPECTROMETRY DATA INDEPENDENTLY GENERATED BY SCRIPPS CENTER FOR METABOLOMICS IS AVAILABLE TO VIEW OR DOWNLOAD IN PDF. A7300.PDF TESTED METABOLITES ARE FEATURED ON SCRIPPS CENTER FOR METABOLOMICS METLIN METABOLITE DATABASE. TO LEARN MORE, VISIT SIGMA.COM/METLIN RTECS: AC6960000 STORAGE TEMPERATURE: -20 DEG C UNSPSC: 12352100 WGK: 3
secure_info
secure_wgk_germany：	3

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