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116632-40-7

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116632-40-7 Usage

Description

1-IODO-2-CHLORO-3-METHYL-BENZENE, with the molecular formula C7H6ClI, is a chemical compound that is a derivative of benzene. It features a chlorine atom at the 2nd position, a methyl group at the 3rd position, and an iodine atom at the 1st position. 1-IODO-2-CHLORO-3-METHYL-BENZENE is known for its applications in various chemical processes and industries.

Uses

Used in Organic Synthesis:
1-IODO-2-CHLORO-3-METHYL-BENZENE is used as a building block in organic synthesis for the creation of more complex organic molecules. Its unique structure with halogen atoms allows for versatile chemical reactions, facilitating the synthesis of a wide range of compounds.
Used as a Precursor in Chemical Production:
In the chemical industry, 1-IODO-2-CHLORO-3-METHYL-BENZENE serves as a precursor to other chemicals, contributing to the formation of various intermediates that are essential in the production of different chemical products.
Used in Pharmaceutical Production:
1-IODO-2-CHLORO-3-METHYL-BENZENE is utilized in the production of pharmaceuticals, where its specific chemical properties are harnessed to create active pharmaceutical ingredients or to facilitate the synthesis of drug molecules.
Used in Agrochemical Production:
1-IODO-2-CHLORO-3-METHYL-BENZENE also finds use in the agrochemical sector, where it may be employed in the synthesis of pesticides, herbicides, or other agricultural chemicals to improve crop protection and yield.
Used in Dye Production:
1-IODO-2-CHLORO-3-METHYL-BENZENE is used in the production of dyes, where its chemical structure contributes to the color and properties of the final dye products.
Used in Materials Science:
With potential applications in materials science, 1-IODO-2-CHLORO-3-METHYL-BENZENE may be incorporated into the development of new materials with specific properties, such as in polymers or composites.
Used as a Reagent in Chemical Reactions:
In the laboratory and industrial settings, 1-IODO-2-CHLORO-3-METHYL-BENZENE functions as a reagent in various chemical reactions, often due to its ability to participate in substitution, addition, or other types of chemical processes.
It is crucial to handle 1-IODO-2-CHLORO-3-METHYL-BENZENE with care due to its hazardous nature, ensuring proper management to mitigate any health risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 116632-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,6,3 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116632-40:
(8*1)+(7*1)+(6*6)+(5*6)+(4*3)+(3*2)+(2*4)+(1*0)=107
107 % 10 = 7
So 116632-40-7 is a valid CAS Registry Number.

116632-40-7SDS

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 2-chloro-1-iodo-3-methylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,2-chloro-1-iodo-3-methyl

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:116632-40-7 SDS

116632-40-7Downstream Products

116632-40-7Relevant articles and documents

Biphenyl compound as well as preparation method and medical application thereof

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, (2020/11/22)

The invention discloses a biphenyl compound as well as a preparation method and medical application thereof, the structure of the biphenyl compound is shown as a formula (I) or a formula (II), and thebiphenyl compound or pharmaceutically acceptable salt, tautomer, meso-isomer, raceme, stereoisomer, metabolite, metabolite precursor, prodrug or solvate thereof is a PD-L1 inhibitor. The compound hasa remarkable inhibiting effect on the interaction of PD-1 and PD-L1 protein, so that the compound can be applied to the preparation of PD-L1 inhibitors and immunomodulator drugs for preventing or treating tumors, autoimmune diseases, organ transplant rejection, infectious diseases and inflammatory diseases.

METHOD OF PRODUCING IODIZING AGENT, AND METHOD OF PRODUCING AROMATIC IODINE COMPOUND

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Page/Page column 11, (2010/05/13)

A method of the present invention, for producing an iodizing agent, includes the step of electrolyzing iodine molecules in a solution by using an acid as a supporting electrolyte. This realizes (i) a method of producing an iodine cation suitable for use as an iodizing agent that does not require a sophisticated separation operation after iodizing reaction is completed, and (ii) an electrolyte used in the method. Further, a method of the present invention, for producing an aromatic iodine compound, includes the step of causing an iodizing agent, and an aromatic compound whose nucleus has one or more substituent groups and two or more hydrogen atoms, to react with each other under the presence of a certain ether compound. This realizes such a method of producing an aromatic iodine compound that position selectivity in iodizing reaction of an aromatic compound is improved.

Pharmaceutical compositions and methods of inhibiting phenylethanolamine N-methyltransferase

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, (2008/06/13)

Pharmaceutical compositions and methods of inhibiting phenylethanolamine N-methyltransferase using 7 and/or 8 substituted 1,2,3,4-tetrahydroisoquinoline compounds.

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