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1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE, also known as 1-chloro-4-iodo-2,5-dimethoxybenzene or 1-(4-chloro-2,5-dimethoxyphenyl)-4-iodobenzene, is a chemical compound with the molecular formula C8H8ClIO2. It is a derivative of benzene with chlorine and iodine atoms attached to different carbon positions and two methoxy groups attached to the benzene ring. 1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE is characterized by its white to off-white solid appearance, a molecular weight of 310.51 g/mol, and a melting point of 131-134°C. Due to its potential for causing skin and eye irritation, it is crucial to handle 1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE with care and follow proper safety protocols.

90064-46-3

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90064-46-3 Usage

Uses

Used in Pharmaceutical Industry:
1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex molecular structures that can exhibit therapeutic properties.
Used in Organic Materials Synthesis:
1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE serves as a building block for various heterocyclic compounds, which are essential in the development of organic materials with specific properties and applications.
Used in Chemical Research:
1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE is utilized in chemical research to explore its reactivity and potential applications in the synthesis of new compounds and materials, further expanding its utility in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 90064-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,6 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90064-46:
(7*9)+(6*0)+(5*0)+(4*6)+(3*4)+(2*4)+(1*6)=113
113 % 10 = 3
So 90064-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClIO2/c1-11-7-4-6(10)8(12-2)3-5(7)9/h3-4H,1-2H3

90064-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Chloro-4-iodo-2,5-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 1-Chlor-4-jod-2,5-dimethoxy-benzol

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 -
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More Details:90064-46-3 SDS

90064-46-3Relevant academic research and scientific papers

A facile synthesis of 1,4-dialkoxy-2,5-diiodobenzenes: reaction of dialkoxybenzenes with iodine monochloride in alcoholic solvents

Wariishi, Koji,Morishima, Sin-Ichi,Inagaki, Yoshio

, p. 98 - 100 (2013/09/05)

A facile synthesis of 1,4-dialkoxy-2,5-diiodobenzenes via diiodination of the corresponding dialkoxybenzenes with iodine monochloride has been developed. Employment of ah alcoholic solvent as a reaction medium is crucial for attaining a high yield; the reaction in a nonalcoholic solvent usually resulted in a poor yield. The diiodobenzene derivatives are useful intermediates in the synthesis of such advanced materiais as soluble phenylenevinylene polymers anal dialkoxy derivatives of 7,7,8,8-tetracyanoquinodimethane.

Multistep Reversible Redox Systems, LXIII. 2,5-Disubstituted N,N'-Dicyanoquinone Diimines (DCNQIs) - Syntheses, and Redox Properties

Huenig, Siegfried,Bau, Robert,Kemmer, Martina,Meixner, Hubert,Metzenthin, Tobias,et al.

, p. 335 - 348 (2007/10/03)

Quinones 1a-q and DCNQIs 2a-g have been synthesized in order to investigate substituent effects.It was necessary to employ novel synthetic routes for the introduction of iodine into 1f (7), the trifluoromethyl group into 1g-i, deuterium into 1m-p, and esp

Radiohalogen-Labeled Imaging Agents. 3. Compounds for Measurement of Brain Blood Flow by Emission Tomography

Sargent, Thornton,Shulgin, Alexander T.,Mathis, Chester A.

, p. 1071 - 1077 (2007/10/02)

The radioiodine-labeled amines currently available as brain-imaging agents, based on our previous work and that of others, are prepared either by exchange labeling or by direct iodination of a protected intermediate.The intrinsic slowness of these process

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