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Benzene, 1-chloro-2-iodyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65386-94-9

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65386-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65386-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,8 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65386-94:
(7*6)+(6*5)+(5*3)+(4*8)+(3*6)+(2*9)+(1*4)=159
159 % 10 = 9
So 65386-94-9 is a valid CAS Registry Number.

65386-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-2-iodylbenzene

1.2 Other means of identification

Product number -
Other names 1-chloro-2-iodyl-benzene

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:65386-94-9 SDS

65386-94-9Upstream product

65386-94-9Downstream Products

65386-94-9Relevant academic research and scientific papers

Mild and efficient synthesis of iodylarenes using Oxone as oxidant

Soldatova, Natalia,Postnikov, Pavel,Troyan, Anna A.,Yoshimura, Akira,Yusubov, Mekhman S.,Zhdankin, Viktor V.

, p. 4254 - 4256 (2016)

Mild and efficient method for the preparation of iodylarenes by oxidation of iodoarenes with Oxone in aqueous acetonitrile at room temperature is described. This new procedure allows the preparation of various iodylarenes with electron-donating or electron-withdrawing substituents in the aromatic ring including the previously unknown 1,2-diiodylbenzene.

Transition metal-mediated oxidations utilizing monomeric iodosyl- and iodylarene species

Yusubov, Mekhman S.,Nemykin, Victor N.,Zhdankin, Viktor V.

experimental part, p. 5745 - 5752 (2010/10/02)

Several transition metal-mediated oxidations using hypervalent iodine species are reported. A convenient procedure for preparation of iodylarenes via RuCl3-catalyzed oxidation of iodoarenes has been developed. This procedure allows the generation of highly reactive monomeric iodine(V) species, which are excellent oxidants toward alcohols and hydrocarbons in situ. A broad range of substrates can be oxidized to carbonyl compounds by a tandem catalytic system based on the Ru(III)-catalyzed reoxidation of ArIO to ArIO2 using Oxone as oxidant. It was shown that electrophilic iodine(III) species, originating from oligomeric iodosylbenzene sulfate (PhIO)3SO3, are efficient oxygenating agents in catalytic oxidation of aromatic hydrocarbons in the presence of metalloporphyrin complexes.

RuCl3-catalyzed oxidation of iodoarenes with peracetic acid: New facile preparation of iodylarenes

Koposov, Alexey Y.,Karimov, Rashad R.,Pronin, Andrey A.,Skrupskaya, Tatyana,Yusubov, Mekhman S.,Zhdankin, Viktor V.

, p. 9912 - 9914 (2007/10/03)

New facile methodology for the preparation of pentavalent iodine compounds using peracetic acid as an oxidant in the presence of catalytic amounts of ruthenium trichloride is described. The new procedure allows the preparation of several previously unknown iodylarenes bearing strongly electron-withdrawing CF3 groups in the aromatic ring.

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