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1,4-Cyclohexadiene, 1,4-diiodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68882-62-2

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68882-62-2 Usage

Physical state

Colorless liquid

Molecular weight

353.94 g/mol

Uses

a. Reagent in organic synthesis
b. Preparation of iodinated compounds
c. Study of molecular structure and reactions

Potential applications

a. Pharmaceuticals
b. Agrochemicals
c. Materials science

Chemical properties

Unique reactivity

Safety precautions

Handle with care due to toxicity and potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 68882-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,8 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68882-62:
(7*6)+(6*8)+(5*8)+(4*8)+(3*2)+(2*6)+(1*2)=182
182 % 10 = 2
So 68882-62-2 is a valid CAS Registry Number.

68882-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-diiodo-1,4-cyclohexadiene

1.2 Other means of identification

Product number -
Other names 1,4-Diiodcyclohexa-1,4-dien

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:68882-62-2 SDS

68882-62-2Downstream Products

68882-62-2Relevant academic research and scientific papers

STUDIES ON THE OXIDATION OF HYDRAZONES WITH IODINE AND WITH PHENYLSELENENYL BROMIDE IN THE PRESENCE OF STRONG ORGANIC BASES; AN IMPROVED PROCEDURE FOR THE SYNTHESIS OF VINYL IODIDES AND PHENYL-VINYL SELENIDES

Barton, Derek H. R.,Bashiardes, George,Fourrey, Jan-Louis

, p. 147 - 162 (2007/10/02)

The oxidation of hydrazones by iodine in the presence of strong organic bases (guanidines) has been studied.Improved yields of vinyl iodides can be obtained by inverse addition using dry solvents and with a final heating period where appropriate.The reaction has been extended to various dihydrazones with interesting results.In complementary studies hydrazones have been oxidized by phenylselenyl bromide in the presence of strong organic bases to give the corresponding phenyl vinyl selenides in good yield.

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