4-Iodophthalonitrile

Suppliers

Names

[ CAS No. ]:
69518-17-8

[ Name ]:
4-Iodophthalonitrile

[Synonym ]:
1,2-dicyano-4-iodobenzene
1,2-Benzenedicarbonitrile, 4-iodo-
4-Iodophthalonitrile
4-I-phthalodinitrile
4-iodo-1,2-dicyanobenzene
MFCD01863730
4-iodophthanitrile

Chemical & Physical Properties

[ Density]:
2.0±0.1 g/cm3

[ Boiling Point ]:
364.7±37.0 °C at 760 mmHg

[ Melting Point ]:
140-142ºC(lit.)

[ Molecular Formula ]:
C8H3IN2

[ Molecular Weight ]:
254.027

[ Flash Point ]:
174.4±26.5 °C

[ Exact Mass ]:
253.934082

[ PSA ]:
47.58000

[ LogP ]:
2.16

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.676

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H312-H315-H319-H332-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
20/21/22-36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2926909090

Synthetic Route

Precursor & DownStream

Precursor

  • 4-Aminophthalonitrile
  • 4-Nitrophthalonitrile
  • 4-Nitrophthaldiamide

DownStream

  • 4-(3-hydroxy-3-methylbut-1-ynyl)benzene-1,2-dicarbonitrile
  • 5-[8-(1-amino-3-iminoisoindol-5-yl)anthracen-1-yl]-3-iminoisoindol-1-amine

Customs

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Novel perfluoroalkyl phthalocyanine metal derivatives: Synthesis and photodynamic activities. Qiu T, et al.

Dyes and Pigments 83(1) , 127-133, (2009)

Alkynyl substituted phthalocyanine derivatives as targets for optical limiting García-Frutos EM, et al.

J. Mater. Chem. 13(4) , 749-753, (2003)

The synthesis of a fluorinated phthalocyanine. Keller TM and Griffith JR.

J. Fluor. Chem. 13(1) , 73-77, (1979)


More Articles


Related Compounds

  • 4-Amino-2-chloro-5-(1H-tetrazol-5-yl)benzenesulfonamide
  • 4-(4-Chlorophenyl)-4-Bromopiperide
  • 4-(2-nitroimidazol-1-yl)butane-1,2-diol
  • 4-Iodo-1H-indazole-3-carboxylic acid
  • 4-chlorooxolan-3-ol,formic acid
  • 4,6-Pyrimidinedicarboxylic acid
  • 2-{1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoyl]-4-methylpyrrolidin-3-yl}acetic acid
  • 2-{1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoyl]-4-methylpyrrolidin-3-yl}acetic acid
  • 2-{1-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoyl]-4-methylpyrrolidin-3-yl}acetic acid
  • 2-{1-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoyl]-4-methylpyrrolidin-3-yl}acetic acid
  • 2-{1-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanoyl]-4-methylpyrrolidin-3-yl}acetic acid
  • 2-{[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1-methyl-1H-pyrazol-5-yl]formamido}pent-4-ynoic acid
  • 1-(5-Bromo-2-methylphenyl)-2,2-dichloroethanol
  • 5-(1-bromopropan-2-yl)-1,3-dimethyl-1H-pyrazole
  • 1,1-Difluoro-3-(2-fluoro-4-methylphenyl)-2-methylpropan-2-amine
  • 3-(Pyrimidin-5-yl)but-3-en-1-amine
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