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2-IODO-ISOPHTHALIC ACID DIMETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106589-18-8

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106589-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106589-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,8 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 106589-18:
(8*1)+(7*0)+(6*6)+(5*5)+(4*8)+(3*9)+(2*1)+(1*8)=138
138 % 10 = 8
So 106589-18-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H9IO4/c1-14-9(12)6-4-3-5-7(8(6)11)10(13)15-2/h3-5H,1-2H3

106589-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-iodobenzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2-iodo-isophthalic acid dimethyl ester

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:106589-18-8 SDS

106589-18-8Relevant academic research and scientific papers

Esters of 2-iodoxybenzoic acid: Hypervalent iodine oxidizing reagents with a pseudobenziodoxole structure

Zhdankin, Viktor V.,Koposov, Alexey Y.,Litvinov, Dmitry N.,Ferguson, Michael J.,McDonald, Robert,Luu, Thanh,Tykwinski, Rik R.

, p. 6484 - 6491 (2005)

Esters of 2-iodoxybenzoic acid (IBX-esters) were prepared by the hypochlorite oxidation of the corresponding 2-iodobenzoate esters and isolated as chemically stable, microcrystalline products. These hypervalent iodine compounds are potentially valuable ox

Synthesis, Structures, and Properties of Neutral and Radical Cationic S,C,C-Bridged Triphenylamines

Kato, Shin-ichiro,Matsuoka, Takanori,Suzuki, Shuichi,Asano, Motoko S.,Yoshihara, Toshitada,Tobita, Seiji,Matsumoto, Taisuke,Kitamura, Chitoshi

, p. 734 - 738 (2020)

A structurally constrained S,C,C-bridged triphenylamine was synthesized, and the corresponding radical cation was obtained as a hexachloroantimonate by chemical oxidation. An X-ray crystallographic analysis revealed an almost planar structure for this rad

Synthesis, characterization, and initial reaction study of two new bicyclic hypervalent iodine(III) reagents

Gao, Wen-Chao,Zhang, Chi

, p. 2687 - 2690 (2014/05/06)

The synthesis of two new bicyclic hypervalent iodine(III) reagents 5 and 6 is described along with their corresponding X-ray crystal structures for the first time. A detailed comparison in the bond lengths and bond angles of reported bicyclic hypervalent

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