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516139

4-Chloro-2-iodoaniline

Name: 4-Chloro-2-iodoaniline
Brand: ALDRICH

98%

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About This Item

Linear Formula:

ClC₆H₃(I)NH₂

CAS Number:

63069-48-7

Molecular Weight:

253.47

EC Number:

263-839-3

MDL number:

MFCD01863737

UNSPSC Code:

12352100

PubChem Substance ID:

24873867

NACRES:

NA.22

Assay

98%

mp

39-43 °C (lit.)

SMILES string

Nc1ccc(Cl)cc1I

InChI

1S/C6H5ClIN/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2

InChI key

FLEJOBRWKBPUOX-UHFFFAOYSA-N

Pictograms

GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H315,H318,H335

Precautionary Statements

P261 - P264 - P280 - P301 + P310 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

>228.2 °F - closed cup

Flash Point(C)

> 109 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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 Journal of Organic Chemistry, 24, 4607-4613 (2001)

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

Wing S Cheung et al.

The Journal of organic chemistry, 70(9), 3741-3744 (2005-04-23)

[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 sequence is presented. Factors influencing yield and selectivity, namely catalyst, coordinating ligand, and solvent, are detailed.

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

A Rosowsky et al.

Journal of medicinal chemistry, 13(5), 882-886 (1970-09-01)

Regioselective iodination of aryl amines using 1, 4-dibenzyl-1, 4-diazoniabicyclo [2.2. 2] octane dichloroiodate in solution and under solvent-free conditions.

Alikarami M, et al.

Bulletin of the Chemical Society of Ethiopia, 29(1), 157-162 (2015)

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