98507-06-3

Basic information

• Product Name: 2,5-DIMETHYL-2,5-CYCLOHEXADIENE-1,4-DIYLIDENEBISCYANAMIDE
• Synonyms: N,N'-(2,5-DIMETHYL-2,5-CYCLOHEXADIENE-1,4-DIYLIDENE)BISCYANAMIDE;N,N'-DICYANO-2,5-DIMETHYLBENZOQUINONEDIIMINE;N N'-DICYANO-2 5-DIMETHYLBENZOQUINONE &;1,4-Bis(cyanoimino)-2,5-dimethyl-2,5-cyclohexadiene;2,5-Dimethyl-1,4-bis(cyanoimino)-2,5-cyclohexadiene;2,5-Dimethyl-N,N'-dicyano-1,4-benzoquinone diimine;2,5-Dimethyl-N,N'-dicyano-p-benzoquinone diimine;N,N'-Dicyano-3,6-dimethyl-p-benzoquinone diimine
• CAS NO: 98507-06-3
• Molecular Formula: C₁₀H₈N₄
• Molecular Weight: 184.2
• Mol File: 98507-06-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 191-194 °C(lit.)
• Appearance: /
• CAS DataBase Reference: 2,5-DIMETHYL-2,5-CYCLOHEXADIENE-1,4-DIYLIDENEBISCYANAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-DIMETHYL-2,5-CYCLOHEXADIENE-1,4-DIYLIDENEBISCYANAMIDE(98507-06-3)
• EPA Substance Registry System: 2,5-DIMETHYL-2,5-CYCLOHEXADIENE-1,4-DIYLIDENEBISCYANAMIDE(98507-06-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• F: 8-10-23
• Hazardous Substances Data: 98507-06-3(Hazardous Substances Data)

Usage

General Description

2,5-DIMETHYL-2,5-CYCLOHEXADIENE-1,4-DIYLIDENEBISCYANAMIDE is a chemical compound with the molecular formula C14H16N4. It is a highly reactive compound that is used in various industrial applications, including in the production of pharmaceuticals, dyes, and polymers. It is also used as a reagent in organic chemistry reactions. The compound is known for its ability to form strong covalent bonds with other molecules, making it useful in the synthesis of new chemical compounds. It is important to handle this compound with care, as it may pose health and environmental risks due to its reactivity and potential toxicity.

Upstream product

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Relevant articles and documents

Chemical states of Ag in Ag(DMe-DCNQI)2 photoproducts and a proposal for its photoinduced conductivity change mechanism

UV-vis light converts Ag(DM)2 (DM = 2,5-dimethylN,N′- dicyanoquionediimine; DMe-DCNQI) to several solids with metallic, semiconducting, or insulating conductivities depending on the irradiation conditions. Ag valence state in each photochemical product was determined by Ag L3-edge XANES. The XANES result requires the correction of the redox mechanism to explain the photoinduced conductivity change of Ag(DM)2 photoproducts. Copyright

Charge transfer complexes of tetrathio/seleno-fulvalene derivatives and biscyanimine derivatives; biscyanimine derivatives and method for producing same

A novel charge transfer complex of an N,N'-biscyanoquinone bisimine of the formula STR1 and a fulvalene derivative of the formula STR2 where, in formula I, R1, R2, R3 and R4 independently of one another are --H,