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4-Iodotoluene

Names

[ CAS No. ]:
624-31-7

[ Name ]:
4-Iodotoluene

[Synonym ]:
p-Methyliodobenzene
4-IODO-TOLUENE
Toluene,p-iodo
4-Iodotoluene
Benzene, 1-iodo-4-methyl-
4-methyliodobenzene
1-Methyl-4-iodobenzene
Benzene,1-iodo-4-methyl
4-iodo-1-methylbenzene
p-Tolyl iodide
p-Iodotoluene
4-methyl-1-iodobenzene
MFCD00001059
1-Iodo-4-methylbenzene
Toluene, p-iodo-
EINECS 210-841-7
4-methylphenyl iodide
para-methyl-iodo-benzene

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
211.5±0.0 °C at 760 mmHg

[ Melting Point ]:
33-35 °C(lit.)

[ Molecular Formula ]:
C7H7I

[ Molecular Weight ]:
218.035

[ Flash Point ]:
90.0±0.0 °C

[ Exact Mass ]:
217.959229

[ LogP ]:
3.71

[ Vapour Pressure ]:
0.3±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.605

[ Water Solubility ]:
insoluble

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29036990

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2903999090

[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Rational strategy for shaped nanomaterial synthesis in reverse micelle reactors.

Nat. Commun. 5 , 3870, (2014)

The shape-controlled synthesis of nanoparticles was established in single-phase solutions by controlling growth directions of crystalline facets on seed nanocrystals kinetically; however, it was diffi...

Transition metal complexes bearing NHC ligands substituted with secondary polyfluoroalkyl groups.

Dalton Trans. 44 , 19663-73, (2015)

Using three different approaches, racemic 1-(perfluoroalkyl)ethylamines were synthesized from perfluoroalkyl iodides or perfluoroalkanoic acids, and further transformed to the corresponding N,N'-disub...

Cobalt-catalyzed aryl-sulfur bond formation.

Org. Lett. 8 , 5613, (2006)

A new cobalt-catalyzed coupling of aryl halides with thiophenols and alkanethiols is reported. A variety of aryl sulfides can be prepared in excellent yields under mild reaction conditions using 1-2 m...


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Related Compounds

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