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84483-28-3

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84483-28-3 Usage

General Description

2-Chloro-6-iodoaniline is a chemical compound with the molecular formula C6H5ClIN. It is a derivative of aniline, a common aromatic amine, with chlorine and iodine substituents at the 2nd and 6th positions, respectively, on the benzene ring. 2-Chloro-6-iodoaniline is used as an intermediate in the synthesis of various pharmaceuticals and organic molecules, as well as in the production of dyes and pigments. It is a potentially hazardous chemical and should be handled and stored with appropriate safety measures. The compound is typically produced through the reaction of aniline with chloramine and then further treated with sodium iodide to introduce the iodine substitution.

Check Digit Verification of cas no

The CAS Registry Mumber 84483-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,8 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84483-28:
(7*8)+(6*4)+(5*4)+(4*8)+(3*3)+(2*2)+(1*8)=153
153 % 10 = 3
So 84483-28-3 is a valid CAS Registry Number.

84483-28-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-6-iodoaniline

1.2 Other means of identification

Product number -
Other names chloroiodoaniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:84483-28-3 SDS

84483-28-3Relevant articles and documents

Synthesis and Investigation of the Abiotic Formation of Pyonitrins A-D

Aniebok, Victor,Lee, Hsiau-Wei,Macmillan, John B.,Shingare, Rahul D.

supporting information, (2020/02/22)

Pyonitrins A-D are recently isolated natural products from the insect-associated Pseudomonas protegens strain, which were isolated from complex fractions that exhibited antifungal activity via an in vivo murine candidiasis assay. Genomic studies of Pseudomonas protegens suggested that pyonitrins A-D are formed via a spontaneous nonenzymatic reaction between biosynthetic intermediates of two well-known natural products pyochelin and pyrrolnitrin. Herein we have accomplished the first biomimetic total synthesis of pyonitrins A-D in three steps and studied the nonenzymatic formation of the pyonitrins using 15N NMR spectroscopy.

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