136272-31-6 Usage
Uses
Used in Agrochemical Production:
5-chloro-1,3-difluoro-2-nitrobenzene is used as an intermediate in the production of agrochemicals. It serves as a key component in the synthesis of various pesticides and herbicides, contributing to their effectiveness in controlling pests and unwanted plant growth.
Used in Pharmaceutical Synthesis:
5-chloro-1,3-difluoro-2-nitrobenzene is also utilized in the synthesis of pharmaceuticals, where it acts as a crucial intermediate in the development of new drugs. Its unique structure allows for the creation of molecules with specific therapeutic properties.
Used in Specialty Chemicals Synthesis:
5-chloro-1,3-difluoro-2-nitrobenzene is employed in the synthesis of specialty chemicals, which are high-value compounds used in various industries such as plastics, coatings, and textiles. Its versatility in chemical reactions makes it a valuable building block for these applications.
Used in Research and Development:
In the field of research and development, 5-chloro-1,3-difluoro-2-nitrobenzene is used to explore new materials and chemical processes. Its reactivity and potential to form various derivatives make it an important tool for scientific investigation and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 136272-31-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,7 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136272-31:
(8*1)+(7*3)+(6*6)+(5*2)+(4*7)+(3*2)+(2*3)+(1*1)=116
116 % 10 = 6
So 136272-31-6 is a valid CAS Registry Number.
136272-31-6Relevant academic research and scientific papers
RADICAL-ANIONS OF AROMATIC COMPOUNDS. XXI. THE RADICAL-ANIONS OF 4-SUBSTITUTED 2,6-DIFLUORO- AND 2,3,5,6-TETRAFLUORONITROBENZENES
Selivanova, G. A.,Starichenko, V. F.,Ryabinin, V. A.,Shteingarts, V. D.
, p. 1140 - 1147 (2007/10/02)
For the radical-anions of the series of 4-substituted nitrobenzenes it was established that it fluorine atoms are introduced at both ortho positions of the nitro group the sensitivity of the nature of the para substituent is increased for the spin-spin co
