83094-62-6 Usage
Uses
Used in Chemical Synthesis Industry:
1H-Indene, 2-chloro-2,3-dihydrois used as an intermediate for the production of various synthetic chemicals, contributing to the creation of a wide range of products in this industry.
Used as a Chemical Reagent in Organic Synthesis:
In the field of organic synthesis, 1H-Indene, 2-chloro-2,3-dihydrois utilized as a chemical reagent, playing a crucial role in various chemical reactions and processes.
Used in Pharmaceutical Production:
1H-Indene, 2-chloro-2,3-dihydroserves as a starting material for the production of pharmaceuticals, aiding in the development and manufacturing of diverse medicinal products.
Used in Agrochemical Production:
1H-Indene, 2-chloro-2,3-dihydrois also employed as a starting material in the production of agrochemicals, which are essential for agricultural applications to enhance crop protection and productivity.
Used in Specialty Chemicals Production:
Furthermore, 1H-Indene, 2-chloro-2,3-dihydro- is used in the production of specialty chemicals, which are important for specific industries that require unique chemical properties for their applications.
Check Digit Verification of cas no
The CAS Registry Mumber 83094-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,9 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83094-62:
(7*8)+(6*3)+(5*0)+(4*9)+(3*4)+(2*6)+(1*2)=136
136 % 10 = 6
So 83094-62-6 is a valid CAS Registry Number.
83094-62-6Relevant academic research and scientific papers
Thiourea-Mediated Halogenation of Alcohols
Mohite, Amar R.,Phatake, Ravindra S.,Dubey, Pooja,Agbaria, Mohamed,Shames, Alexander I.,Lemcoff, N. Gabriel,Reany, Ofer
supporting information, p. 12901 - 12911 (2020/11/26)
The halogenation of alcohols under mild conditions expedited by the presence of substoichiometric amounts of thiourea additives is presented. The amount of thiourea added dictates the pathway of the reaction, which may diverge from the desired halogenation reaction toward oxidation of the alcohol, in the absence of thiourea, or toward starting material recovery when excess thiourea is used. Both bromination and chlorination were highly efficient for primary, secondary, tertiary, and benzyl alcohols and tolerate a broad range of functional groups. Detailed electron paramagnetic resonance (EPR) studies, isotopic labeling, and other control experiments suggest a radical-based mechanism. The fact that the reaction is carried out at ambient conditions, uses ubiquitous and inexpensive reagents, boasts a wide scope, and can be made highly atom economic, makes this new methodology a very appealing option for this archetypical organic reaction.
