Global Information Lookup Global Information

Phthalonitrile information


Phthalonitrile
Skeletal formula
Space-filling model
Names
Preferred IUPAC name
Benzene-1,2-dicarbonitrile[1]
Other names
Phthalonitrile[1]
Phthalodinitrile
1,2-Benzenedicarbonitrile
1,2-Dicyanobenzene
Identifiers
CAS Number
  • 91-15-6 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 6775 checkY
ECHA InfoCard 100.001.859 Edit this at Wikidata
PubChem CID
  • 7042
UNII
  • 978627YAJU checkY
CompTox Dashboard (EPA)
  • DTXSID8029604 Edit this at Wikidata
InChI
  • InChI=1S/C8H4N2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H checkY
    Key: XQZYPMVTSDWCCE-UHFFFAOYSA-N checkY
  • InChI=1/C8H4N2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H
    Key: XQZYPMVTSDWCCE-UHFFFAOYAX
SMILES
  • N#Cc1ccccc1C#N
Properties
Chemical formula
C6H4(CN)2
Molar mass 128.13 g/mol
Appearance Off-white crystals with lumps on the surface.
Odor Almond-like
Density 1.238 g/cm3[2]
Melting point 139 to 141 °C (282 to 286 °F; 412 to 414 K)
Boiling point sublimes
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Phthalonitrile is an organic compound with the formula C6H4(CN)2, which is an off-white crystal solid at room temperature. It is a derivative of benzene, containing two adjacent nitrile groups. The compound has low solubility in water but is soluble in common organic solvents. The compound is used as a precursor to phthalocyanine and other pigments, fluorescent brighteners, and photographic sensitizers.

  1. ^ a b Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 902. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  2. ^ Cite error: The named reference ullmann was invoked but never defined (see the help page).

and 15 Related for: Phthalonitrile information

Request time (Page generated in 0.5164 seconds.)

Phthalonitrile

Last Update:

Phthalonitrile is an organic compound with the formula C6H4(CN)2, which is an off-white crystal solid at room temperature. It is a derivative of benzene...

Word Count : 390

Copper phthalocyanine

Last Update:

copper(I) cyanide and o-dibromobenzene, which mainly produces colorless phthalonitrile as well as an intensely blue by-product. A couple of years later, workers...

Word Count : 2209

Pigment yellow 139

Last Update:

insoluble in most solvents. It is prepared by addition of ammonia to phthalonitrile to give diiminoisoindole, which in turn condenses with barbituric acid...

Word Count : 121

Phthalocyanine

Last Update:

octamethylphthalocyanine in an attempted conversion of o-dibromobenzene into phthalonitrile. They remarked on the enormous stability of these complexes but did...

Word Count : 1661

Pigment yellow 185

Last Update:

isoindoline. This yellow green compound is prepared by addition of ammonia to phthalonitrile to give diiminoisoindole, which in turn condenses first with N-methylcyanoacetamide...

Word Count : 92

Isophthalonitrile

Last Update:

organic compound with the formula C6H4(CN)2. Two other isomers exist, phthalonitrile and terephthalonitrile. All three isomers are produced commercially...

Word Count : 95

Nitrile

Last Update:

acetonitrile. On an industrial scale, several derivatives of benzonitrile, phthalonitrile, as well as Isobutyronitrile are prepared by ammoxidation. The process...

Word Count : 3472

C8H4N2

Last Update:

C8H4N2 (molar mass: 128.13 g/mol, exact mass: 128.0374 u) may refer to: Phthalonitrile, or phthalodinitrile Isophthalonitrile 1,4-Dicyanobenzene This set index...

Word Count : 59

List of compounds with carbon number 8

Last Update:

C8H4FeO4 cyclobutadienecarboxaldehydeiron tricarbonyl 33056-62-1 C8H4N2 phthalonitrile 91-15-6 C8H4N2S2 bitoscanate 4044-65-9 C8H4O3 phthalic anhydride 85-44-9...

Word Count : 28

Ammoxidation

Last Update:

weakness of their C-H bonds. Benzonitrile is produced from toluene, and phthalonitriles are produced from xylenes. The reaction represents a partial oxidation...

Word Count : 518

Reghunadhan Nair

Last Update:

Satheesh Chandran, D Mathew and C.P. Reghunadhan Nair*, "High Performance Phthalonitrile Resins: Challenges and Engineering Applications, Publishers, Walter...

Word Count : 500

Porphyrazine

Last Update:

magnesium templated cyclization of maleonitriles. Cross-cyclization with phthalonitrile or diiminoisoindole derivatives is possible introducing a flexibile...

Word Count : 632

Takuzo Aida

Last Update:

propagating chain serves as a template to catalyze the conversion of phthalonitriles into phthalocyanines in an exceptionally high yield of over 80%. Solvent-free...

Word Count : 4861

Wheat diseases

Last Update:

pyrazole-carboxamide oxycarboxin, oxathiin-carboxamide Strobylurines kresoxim-methyl Phthalonitriles chlorothalonil "Wheat disease management guide" (PDF). HGCA, Agriculture...

Word Count : 629

Template reaction

Last Update:

Phthalocyanines are generated by metal-templated condensations of phthalonitriles, but the liberation of metal-free phthalocyanine is difficult. Some...

Word Count : 630

PDF Search Engine © AllGlobal.net