124251-43-0

Basic information

• Product Name: 4-(n-butylamino)-6-(n-butylimino)-3-oxocyclohexa-1,4-dien-1-olate
• Synonyms: 4-(n-butylamino)-6-(n-butylimino)-3-oxocyclohexa-1,4-dien-1-olate
• CAS NO: 124251-43-0
• Molecular Weight: 250.341
• Mol File: 124251-43-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-(n-butylamino)-6-(n-butylimino)-3-oxocyclohexa-1,4-dien-1-olate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(n-butylamino)-6-(n-butylimino)-3-oxocyclohexa-1,4-dien-1-olate(124251-43-0)
• EPA Substance Registry System: 4-(n-butylamino)-6-(n-butylimino)-3-oxocyclohexa-1,4-dien-1-olate(124251-43-0)

Safety Data

• Hazardous Substances Data: 124251-43-0(Hazardous Substances Data)

Upstream product

• 533-73-3 1,2,4-Trihydroxybenzene 
• 109-73-9 N-butylamine 
• 16523-31-2 4,6-diaminoresorcin dihydrochloride 
• 119014-47-0 2-amino-5-hydroxy-[1,4]benzoquinone-4-imine 
• 120-80-9 benzene-1,2-diol 

Downstream Products

• 1132799-35-9 [(1,1'-bis(diphenylphosphino)ferrocene)Cu(N,N'-di-n-butyl-2-amino-5-alcoholate-1,4-benzoquinonemonoiminium(-1H))] 
• 1263816-26-7 [Pd(II)(azobenzene(-H))(4-(n-butylamino)-6-(n-butylimino)-3-oxocyclohexa-1,4-dien-1-olate^(1-))] 
• 1357474-72-6 [Ru(PPh₃)2(H)(CO)(4-(n-butylamino)-4-(n-butylimino)-3-oxocyclohexa-1,4-dien-1-olate)] 

Relevant articles and documents

Reactivity of TCNE or TCNQ derivatives of quinonoid zwitterions: Platinum-induced HCN elimination vs oxidative-addition

The reaction of the functional, zwitterionic quinonoid molecule (6E)-4-(butylamino)-6-(butyliminio)-3-oxo-2-(1,1,2,2-tetracyanoethyl) cyclohexa-1,4-dien-1-olate, [C6H-2-{C(CN)2C(CN) 2H}]-4,6-(???NH n-Bu)2-1, 3(?

Rapid and facile solvent-free mechanosynthesis in a cell lysis mill: Preparation and mechanochemical complexation of aminobenzoquinones

A cell lysis mill, typically used for the breakdown of biological structures in microbiological and biochemical studies, was used as a tool for rapid, solvent-free and general synthesis of short- and long-chain substituted zwitterionic meta- and para-amin

Addition of Aliphatic and Aromatic Amines to Catechol in Aqueous Solution Under Oxidizing Conditions

The oxidation of catechol in the presence of two aliphatic and aromatic amines has been investigated.In aqueous solutions of pH 7.0 and 11.7, the substitution pattern of the adduct was dependent on the type of amine used.Aromatic amines produced 4,5-disub