64037-24-7 Usage
Uses
Used in Pharmaceutical Research:
5-Chloro-N-methyl-2-benzoxazolamine is employed as a research compound for exploring its potential pharmacological properties. Its unique structure and functional groups make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
In the chemical industry, 5-Chloro-N-methyl-2-benzoxazolamine is used as an intermediate in the synthesis of various organic compounds and pharmaceuticals. Its reactivity and functional groups allow for the formation of a wide range of derivatives with diverse applications.
Used in Material Science:
5-Chloro-N-methyl-2-benzoxazolamine may also find applications in material science, where its unique chemical properties can be leveraged to develop new materials with specific characteristics, such as improved stability, reactivity, or selectivity.
Used in Analytical Chemistry:
As an analytical reagent, 5-Chloro-N-methyl-2-benzoxazolamine can be utilized in various analytical techniques to detect, quantify, or separate specific compounds or elements. Its unique chemical properties may offer advantages in selectivity, sensitivity, or specificity compared to other reagents.
Used in Environmental Applications:
5-Chloro-N-methyl-2-benzoxazolamine may also have potential applications in environmental science, such as in the detection or remediation of pollutants, or in the development of environmentally friendly materials and processes. Its unique chemical properties could contribute to innovative solutions for environmental challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 64037-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,3 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64037-24:
(7*6)+(6*4)+(5*0)+(4*3)+(3*7)+(2*2)+(1*4)=107
107 % 10 = 7
So 64037-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClN2O/c1-10-8-11-6-4-5(9)2-3-7(6)12-8/h2-4H,1H3,(H,10,11)
64037-24-7Relevant academic research and scientific papers
Utility of Nitrogen Extrusion of Azido Complexes for the Synthesis of Nitriles, Benzoxazoles, and Benzisoxazoles
Nimnual, Phongprapan,Tummatorn, Jumreang,Thongsornkleeb, Charnsak,Ruchirawat, Somsak
, p. 8657 - 8667 (2015/09/15)
The utility of the nitrogen extrusion reaction of azido complexes, generated in situ from the corresponding aldehydes or ketones with TMSN3 in the presence of ZrCl4 or TfOH, has been described. These azido complexes could undergo three different pathways, depending on the substrates. First, azido methanolate complexes or imine diazonium ions could lead to benzisoxazole products via an intramolecular nucleophilic substitution. Second, imine diazonium ions could also undergo either the elimination of proton to provide nitrile products in good to excellent yields or an aryl migration, followed by an intramolecular nucleophilic addition, to give benzoxazole products in good yields.
