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1478-08-6

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1478-08-6 Usage

General Description

1,2,3,4-tetrafluoro-5-iodo-6-(trifluoromethyl)benzene is a chemical compound with the molecular formula C7H2F4I. It is a substituted aromatic compound with four fluorine atoms and one iodine atom attached to a six-carbon benzene ring, as well as a trifluoromethyl group. 1,2,3,4-tetrafluoro-5-iodo-6-(trifluoromethyl)benzene has potential applications in organic synthesis and materials science, such as in the development of new pharmaceuticals or advanced materials. It is important to handle this chemical with care, as it may pose hazards to human health and the environment due to its reactivity and potential toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 1478-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1478-08:
(6*1)+(5*4)+(4*7)+(3*8)+(2*0)+(1*8)=86
86 % 10 = 6
So 1478-08-6 is a valid CAS Registry Number.

1478-08-6SDS

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 1,2,3,4-tetrafluoro-5-iodo-6-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 1,2,3,4-Tetrafluor-5-jod-6-trifluormethylbenzol

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:1478-08-6 SDS

1478-08-6Downstream Products

1478-08-6Relevant articles and documents

Opening of the four-membered ring in perfluorinated 1-alkyl-2-phenyl-and 1-aryl-1,2-dihydrocyclobutabenzenes in the system I2-SbF5

Mezhenkova,Karpov,Platonov

experimental part, p. 1026 - 1034 (2011/10/19)

Reactions of perfluorinated 1-phenyl-, 1-(2-ethylphenyl)-, 1-(4-ethylphenyl)-, 1-methyl-2-phenyl-, and 1-ethyl-2-phenyl-1,2- dihydrocyclobutabenzenes with iodine in antimony pentafluoride at 130°C, followed by hydroysis of the reaction mixture, resulted in the formation of perfluorinated 2-methyl-, 2-ethyl-2′-methyl-, 4-ethyl-2'-methyl-, 2-ethyl-, and 2-propylbenzophenones via opening of the four-membered ring in the initial cyclobutabenzene at the C1-C2 bond. The presence of hydrogen fluoride facilitates the process and promotes profound transformations leading to anthracene derivatives.

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