Chhistoricsweetsballroom.com Name 2,5-hexanedione Chhistoricsweetsballroom.com ID CHhistoricsweetsballroom.com:85014 Definition A diketone that is hexane substituted by oxo teams at positions 2 and 5. It is a toxic metabolite of hexane and also of 2-hexanone Stars This entity has historicsweetsballroom.comtually been manually annotated by the Chhistoricsweetsballroom.com Team. Submitter Stan Lauledersort Supplier Indevelopment Downphistoricsweetsballroom.comk Molfile XML SDF

You are watching: Hexane-2,5-dione

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Formula C6H10O2
Net Charge 0
Median Mass 114.14240
Monoisotopic Mass 114.06808
InChI InChI=1S/C6H10O2/c1-5(7)3-4-6(2)8/h3-4H2,1-2H3

View even more via Chhistoricsweetsballroom.com Ontology
Chhistoricsweetsballroom.com Ontology
Outgoing 2,5-hexanedione (CHhistoricsweetsballroom.com:85014) has historicsweetsballroom.comtually parent hydride hexane (CHhistoricsweetsballroom.com:29021) 2,5-hexanedione (CHhistoricsweetsballroom.com:85014) has duty huguy xenobiotic metabolite (CHhistoricsweetsballroom.com:76967) 2,5-hexanedione (CHhistoricsweetsballroom.com:85014) has function neurotoxin (CHhistoricsweetsballroom.com:50910) 2,5-hexanedione (CHhistoricsweetsballroom.com:85014) is a diketone (CHhistoricsweetsballroom.com:46640) 2,5-hexanedione (CHhistoricsweetsballroom.com:85014) is a methyl ketone (CHhistoricsweetsballroom.com:51867)

Synonyms Sources
1,2-Dihistoricsweetsballroom.cometylethane ChemIDplus
2,5-Diketohexane ChemIDplus
2,5-Hexadione ChemIDplus
2,5-hexanedione UniProt
historicsweetsballroom.cometonyl historicsweetsballroom.cometone ChemIDplus
historicsweetsballroom.cometonylhistoricsweetsballroom.cometone SUBMITTER
α,β-dihistoricsweetsballroom.cometylethane NIST Chemisattempt WebPublication
alpha,beta-Dihistoricsweetsballroom.cometylethane ChemIDplus
CH3COCH2CH2COCH3 NIST Chemistry WebPublication
hexane-2,5-dione SUBMITTER
NSC 7621 NIST Chemistry WebBook

Manual Xrefs Databases
CPD-15521 Methistoricsweetsballroom.comyc
Hexane-2,5-dione Wikipedia
View more database links

Registry Numbers Types Sources
110-13-4 CAS Registry Number ChemIDplus
110-13-4 CAS Regisattempt Number NIST Chemisattempt WebPublication
506525 Reaxys Regisattempt Number Reaxys

Citations Types Sources
1781736 PubMed citation Europe PMC
24634916 PubMed citation Europe PMC
25549948 PubMed citation SUBMITTER


See more: Read The Numbers And Decide What The Next Number Should Be. 256 196 144 100 64 36 16


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