116632-43-0 Usage
Uses
Used in Organic Synthesis:
1-Chloro-3-iodo-5-methyl-benzene is used as an intermediate in organic synthesis for the creation of more complex molecules. Its unique structure allows for further chemical modifications, making it a valuable building block for the development of new compounds with specific properties and functions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-Chloro-3-iodo-5-methyl-benzene is used as a reagent in the synthesis of various drugs. Its presence in the molecular structure can contribute to the pharmacological activity of the final product, enhancing its therapeutic effects.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1-Chloro-3-iodo-5-methyl-benzene serves as a reagent in the production of agrochemicals such as pesticides and herbicides. Its incorporation into these compounds can improve their efficacy in controlling pests and weeds, thus contributing to increased crop yields.
Safety Precautions:
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. Appropriate safety measures, including the use of personal protective equipment and adherence to proper disposal procedures, should be taken to minimize potential hazards.
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.
116632-43-0Relevant 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.
Remarkable sensitivity to DNA base shape in the DNA polymerase active site
Sintim, Herman O.,Kool, Eric T.
, p. 1974 - 1979 (2007/10/03)
(Figure Presented) Shaping up: DNA polymerase I can distinguish easily and with high sensitivity between nucleobases that have the same size but differ in shape. The shape, altered through variation in the position of the halogen substituent(s), plays mor
