1183538-72-8 Usage
Physical Properties
Color: Colorless to pale yellow
Odor: Strong odor
State: Liquid
Industrial Applications
Pharmaceutical Synthesis: Used as a building block in pharmaceutical synthesis.
Agrochemical Synthesis: Employed in the synthesis of agrochemicals.
Dye Synthesis: Utilized in the production of dyes.
Surfactant Production: Used in the manufacturing of surfactants.
Corrosion Inhibitors: Employed in the production of corrosion inhibitors.
Potential Uses
Chelating Agent: Studied for potential use as a chelating agent in metal extraction processes.
Lubricant Additive: Investigated for its potential as an additive in lubricants to enhance thermal stability and anti-wear properties.
Safety Concerns
Toxicity: Considered toxic; therefore, handling and use should be conducted with caution.
Health Hazards: Potential health hazards associated with exposure.
Safety Measures
Appropriate Handling: Requires careful handling.
Safety Precautions: Use appropriate safety measures during handling and use.
Check Digit Verification of cas no
The CAS Registry Mumber 1183538-72-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,3,5,3 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1183538-72:
(9*1)+(8*1)+(7*8)+(6*3)+(5*5)+(4*3)+(3*8)+(2*7)+(1*2)=168
168 % 10 = 8
So 1183538-72-8 is a valid CAS Registry Number.
1183538-72-8Relevant articles and documents
Site-Specific C(sp3)–H Aminations of Imidates and Amidines Enabled by Covalently Tethered Distonic Radical Anions
Fang, Yuanding,Fu, Kang,Shi, Lei,Zhao, Rong,Zhou, Jia
, p. 20682 - 20690 (2020/09/07)
The utilization of N-centered radicals to synthesize nitrogen-containing compounds has attracted considerable attention recently, due to their powerful reactivities and the concomitant construction of C?N bonds. However, the generation and control of N-centered radicals remain particularly challenging. We report a tethering strategy using SOMO-HOMO-converted distonic radical anions for the site-specific aminations of imidates and amidines with aid of the non-covalent interaction. This reaction features a remarkably broad substrate scope and also enables the late-stage functionalization of bioactive molecules. Furthermore, the reaction mechanism is thoroughly investigated through kinetic studies, Raman spectroscopy, electron paramagnetic resonance spectroscopy, and density functional theory calculations, revealing that the aminations likely involve direct homolytic cleavage of N?H bonds and subsequently controllable 1,5 or 1,6 hydrogen atom transfer.
