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116632-43-0

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116632-43-0 Usage

General Description

1-Chloro-3-iodo-5-methyl-benzene is a chemical compound that belongs to the benzene class of aromatic hydrocarbons. It is composed of a benzene ring with a chloro, iodo, and methyl group attached at different positions. 1-Chloro-3-iodo-5-methyl-benzene is primarily used as an intermediate in organic synthesis, where it can be further modified to create more complex molecules for various applications. It is also a valuable reagent in the pharmaceutical and agrochemical industries. Despite its usefulness, 1-Chloro-3-iodo-5-methyl-benzene should be handled with care as it may pose health and environmental risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 116632-43-0 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 116632-43:
(8*1)+(7*1)+(6*6)+(5*6)+(4*3)+(3*2)+(2*4)+(1*3)=110
110 % 10 = 0
So 116632-43-0 is a valid CAS Registry Number.

116632-43-0SDS

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 1-Chloro-3-iodo-5-methylbenzene

1.2 Other means of identification

Product number -
Other names 3-chloranyl-5-iodanyl-pyridine

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:116632-43-0 SDS

116632-43-0Relevant articles and documents

Sterically controlled iodination of arenes via iridium-catalyzed C-H borylation

Partridge, Benjamin M.,Hartwig, John F.

supporting information, p. 140 - 143 (2013/03/28)

A mild method to prepare aryl and heteroaryl iodides by sequential C-H borylation and iodination is reported. The regioselectivity of this process is controlled by steric effects on the C-H borylation step and is complementary to existing methods to form aryl iodides. The iodination of boronic esters has potential for the synthesis of radiolabeled aryl iodides, as demonstrated by the concise synthesis of a potential tracer for SPECT imaging.

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