35552-76-2 Usage
Uses
Used in Pharmaceutical Industry:
N,N-dimethyl-2-Quinoxalinamine is used as a building block for the production of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Dye Industry:
N,N-dimethyl-2-Quinoxalinamine is utilized as an intermediate in the synthesis of dyes, enhancing the color properties and performance of various dye products.
Used in Agrochemical Industry:
N,N-dimethyl-2-Quinoxalinamine is employed in the creation of agrochemicals, playing a crucial role in the development of effective and sustainable agricultural solutions.
Used in Organic Synthesis:
As a synthetic intermediate, N,N-dimethyl-2-Quinoxalinamine is used in the design and synthesis of new materials and organic reactions, expanding the scope of chemical research and development.
Used in Research and Development:
Due to its diverse range of applications and unique chemical properties, N,N-dimethyl-2-Quinoxalinamine serves as a valuable tool for research and development in various fields, driving innovation and advancements in multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 35552-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,5 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35552-76:
(7*3)+(6*5)+(5*5)+(4*5)+(3*2)+(2*7)+(1*6)=122
122 % 10 = 2
So 35552-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3/c1-13(2)10-7-11-8-5-3-4-6-9(8)12-10/h3-7H,1-2H3
35552-76-2Relevant academic research and scientific papers
Simple, efficient protocols for the Pd-catalyzed cross-coupling reaction of aryl chlorides and dimethylamine
Lee, Brian K.,Biscoe, Mark R.,Buchwald, Stephen L.
supporting information; experimental part, p. 3672 - 3674 (2009/10/04)
Simple and efficient procedures for the Pd-catalyzed cross-coupling reaction of aryl chlorides and dimethylamine are described. At room temperature with a strong base, t-BuXPhos is employed as the supporting ligand; at 110 °C with a weak base, XPhos is employed as the supporting ligand. In each of these cases, commercially available solutions constitute the source of the dimethylamine, and recently disclosed precatalysts constitute the source of the ligand and Pd. This work further expands the utility of these precatalysts in reactions that benefit from an easily activated source of L1Pd(0).
