35552-76-2 Usage
General Description
N,N-dimethyl-2-Quinoxalinamine is a chemical compound that is commonly used as an intermediate in the synthesis of various organic compounds. It is a derivative of quinoxaline, a heterocyclic compound containing a benzene ring fused to a pyrazine ring. This chemical is recognized for its diverse range of applications, including its use as a building block in the production of pharmaceuticals, dyes, and agrochemicals. It is also used in the synthesis of synthetic intermediates for organic reactions and in the design of new materials. N,N-dimethyl-2-Quinoxalinamine has the potential to serve as a valuable tool for research and development in various fields due to its unique chemical reactivity and versatility.
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 articles and documents
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).
