2,5-Cyclohexadiene-1,4-dione, O-methyloxime oxime

Base Information

• Chemical Name: 2,5-Cyclohexadiene-1,4-dione, O-methyloxime oxime
• CAS No.: 876-34-6
• Molecular Formula: C₇H₈N₂O₂
• Molecular Weight: 152.153
• DSSTox Substance ID: DTXSID501232235

Synonyms:876-34-6;2,5-Cyclohexadiene-1,4-dione, O-methyloxime oxime;DTXSID501232235

Chemical Property of 2,5-Cyclohexadiene-1,4-dione, O-methyloxime oxime

Chemical Property:

• Melting Point: 116 °C
• PSA: 54.18000
• LogP: 0.94500
• XLogP3: 1.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 152.058577502
• Heavy Atom Count: 11
• Complexity: 122

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CONC1=CC=C(C=C1)N=O

Technology Process of 2,5-Cyclohexadiene-1,4-dione, O-methyloxime oxime

There total 2 articles about 2,5-Cyclohexadiene-1,4-dione, O-methyloxime oxime which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

[1,4]Benzoquinone mono-(O-methyl-oxime) (15312-05-7) → p-benzoquinone dioxime monomethyl ether (876-34-6)

Guidance literature:

With hydrogenchloride; hydroxylamine hydrochloride;

DOI:10.1557/JMR.2000.0125

Reference yield:

→ p-benzoquinone dioxime monomethyl ether (876-34-6)

Guidance literature:

1,4-Benzochinon-monoxim-methylether IIIa, Hydroxylamin-hydrochlorid;

Reference yield:

p-benzoquinone dioxime monomethyl ether (876-34-6) + anthranilic acid (118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4) → 3-methoxy-3-(p-nitrosophenyl)-1-(o-carboxyphenyl)triazene

Guidance literature:

With hydrogenchloride; sodium hydroxide; sodium nitrite; Yield given. Multistep reaction;

upstream raw materials:

[1,4]Benzoquinone mono-(O-methyl-oxime)

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