62492-41-5 Usage
Uses
Used in Pharmaceutical Industry:
1-Chloro-2-Methoxy-5-Methyl-4-nitrobenzene is used as an intermediate in the synthesis of pharmaceuticals for its ability to be a building block for more complex organic molecules, contributing to the development of new drugs.
Used in Dye Industry:
In the dye industry, 1-Chloro-2-Methoxy-5-Methyl-4-nitrobenzene is utilized as a chemical intermediate for the production of various dyes, leveraging its structural components to create a range of colorants.
Used in Agrochemical Industry:
1-Chloro-2-Methoxy-5-Methyl-4-nitrobenzene serves as a precursor in the agrochemical sector, playing a role in the creation of compounds used in pesticides and other agricultural chemicals to protect crops.
Used in Organic Synthesis:
1-Chloro-2-Methoxy-5-Methyl-4-nitrobenzene is also used in organic synthesis as a versatile building block for the assembly of more complex organic molecules, highlighting its importance in the synthesis of a wide array of chemical products.
Safety Note:
It is crucial to handle 1-Chloro-2-Methoxy-5-Methyl-4-nitrobenzene with care due to its toxic nature and potential to cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken to minimize exposure and ensure the well-being of those who work with 1-Chloro-2-Methoxy-5-Methyl-4-nitrobenzene.
Check Digit Verification of cas no
The CAS Registry Mumber 62492-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,9 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62492-41:
(7*6)+(6*2)+(5*4)+(4*9)+(3*2)+(2*4)+(1*1)=125
125 % 10 = 5
So 62492-41-5 is a valid CAS Registry Number.
62492-41-5Relevant academic research and scientific papers
Compounds and methods for doping liquid crystal hosts
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, (2008/06/13)
This invention provides chiral thioindigo compounds for doping smectic liquid crystal hosts, wherein the compounds modulate a chiral bulk property of an induced chiral smectic liquid crystal phase upon irradiation at a wavelength in the visible range. Modulation of the chiral bulk property is effected by reversible trans-cis photoisomerization of the compound upon irradiation. The compounds maintain their rod-like shape in both isomeric forms, and hence do not destabilize the chiral smectic liquid crystal phase. Compounds according to the invention are useful in optical devices such as optical switches, displays, and memory.
