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64248-57-3

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64248-57-3 Usage

General Description

1,2-Difluoro-3-iodo-benzene is a chemical compound with the molecular formula C6H3F2I. It is a derivative of benzene, containing two fluorine atoms and one iodine atom. 1,2-DIFLUORO-3-IODO-BENZENE is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. 1,2-Difluoro-3-iodo-benzene is also employed as a reagent in organic synthesis, particularly in the production of complex organic molecules. It is important to handle this chemical with care due to its potential hazards, including its flammability and toxicity. Overall, 1,2-difluoro-3-iodo-benzene has a variety of applications in the field of chemistry and is an important building block for the synthesis of diverse compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 64248-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,4 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64248-57:
(7*6)+(6*4)+(5*2)+(4*4)+(3*8)+(2*5)+(1*7)=133
133 % 10 = 3
So 64248-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F2I/c7-4-2-1-3-5(9)6(4)8/h1-3H

64248-57-3SDS

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 1,2-difluoro-3-iodobenzene

1.2 Other means of identification

Product number -
Other names 2,3-DI-O-ACETYL-4,6-O-ETHYLIDENE-

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:64248-57-3 SDS

64248-57-3Upstream product

64248-57-3Relevant articles and documents

Enhancing charge mobilities in selectively fluorinated oligophenyl organic semiconductors: a design approach based on experimental and computational perspectives

Maiti, Buddhadev,Wang, Kunlun,Bhandari, Srijana,Bunge, Scott D.,Twieg, Robert J.,Dunietz, Barry D.

supporting information, p. 3881 - 3888 (2019/04/30)

Fluorination can be used to tune optoelectronic properties at the molecular level. A series of oligophenyls with various difluorinations of the phenyl rings has been synthesized, crystalized, structurally resolved and computationally analyzed for charge m

Method for producing tetrakis ( fluoroaryl) borate-magnesium compound

-

, (2008/06/13)

Fluoroaryl magnesium halide is reacted with a boron compound so that a molar ratio of the fluoroaryl magnesium halide to the boron compound is not less than 3.0 and not more than 3.7, so as to produce a tetrakis (fluoroaryl) borate·magnesium compound. With this method, there occurs no hydrogen fluoride which corrodes a producing apparatus and requires troublesome waste water treatment.

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