4-Chloro-2-iodoaniline

[ Density]:
2.0±0.1 g/cm3

[ Boiling Point ]:
295.0±25.0 °C at 760 mmHg

[ Melting Point ]:
40 °C

[ Molecular Formula ]:
C₆H₅ClIN

[ Molecular Weight ]:
253.468

[ Flash Point ]:
132.2±23.2 °C

[ Exact Mass ]:
252.915512

[ PSA ]:
26.02000

[ LogP ]:
2.66

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.694

[ Storage condition ]:
Refrigerated.

Click to get detail MSDS

[ Symbol ]:

GHS05, GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H315-H318-H335

[ Precautionary Statements ]:
P261-P280-P301 + P310-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges

[ Hazard Codes ]:
T:Toxic;N:Dangerousfortheenvironment;

[ Risk Phrases ]:
R25;R37/38;R41;R51/53

[ Safety Phrases ]:
S26-S36/37/39-S61-S45

[ RIDADR ]:
UN 2811

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2921420090

Click to get detail synthetic route

Precursor

DownStream

[ HS Code ]: 2921420090

[ Summary ]:
HS:2921420090 aniline derivatives and their salts VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Quinazolines. VI. Synthesis of 2,4-diaminoquinazolines from anthranilonitriles.

J. Med. Chem. 13(5) , 882-6, (1970)

A tandem Heck-carbocyclization/Suzuki-coupling approach to the stereoselective syntheses of asymmetric 3,3-(diarylmethylene)indolinones.

J. Org. Chem. 70(9) , 3741-4, (2005)

[reaction: see text] An efficient and versatile method for stereoselective synthesis of (E)-3,3-(diarylmethylene)indolinones by a palladium-catalyzed tandem Heck-carbocyclization/Suzuki-coupling seque...

Stereoselective Synthesis of (E)-3-(Methoxycarbonyl) methylene-1, 3-dihydroindol-2-ones by Palladium-Catalyzed Oxidative Carbonylation of 2-Ethynylanilines. Gabriele B, et al.

European J. Org. Chem. 24 , 4607-4613, (2001)

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