137069-23-9 Usage
Uses
Used in Pharmaceutical Industry:
METHYL-(2-M-TOLYL-ETHYL)-AMINE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to serve as a building block in the creation of complex organic molecules, contributing to the development of new drugs and medicinal compounds.
Used in Dye Industry:
In the dye industry, METHYL-(2-M-TOLYL-ETHYL)-AMINE is utilized as a precursor in the production of dyes. Its chemical properties enable it to participate in reactions that yield a range of colorants used in various applications, including textiles, plastics, and printing inks.
Used in Organic Chemicals Production:
METHYL-(2-M-TOLYL-ETHYL)-AMINE is also employed in the synthesis of other organic chemicals. Its versatility in chemical reactions makes it a valuable component in the production of a wide array of specialty chemicals used across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 137069-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,6 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137069-23:
(8*1)+(7*3)+(6*7)+(5*0)+(4*6)+(3*9)+(2*2)+(1*3)=129
129 % 10 = 9
So 137069-23-9 is a valid CAS Registry Number.
137069-23-9Relevant academic research and scientific papers
α-Diazo-β-ketonitriles: Uniquely reactive substrates for arene and alkene cyclopropanation
Nani, Roger R.,Reisman, Sarah E.
, p. 7304 - 7311 (2013/06/27)
An investigation of the intramolecular cyclopropanation reactions of α-diazo-β-ketonitriles is reported. These studies reveal that α-diazo-β-ketonitriles exhibit unique reactivity in their ability to undergo arene cyclopropanation reactions; other similar acceptor-acceptor- substituted diazo substrates instead produce mixtures of C-H insertion and dimerization products. α-Diazo-β-ketonitriles also undergo highly efficient intramolecular cyclopropanation of tri- and tetrasubstituted alkenes. In addition, the α-cyano-α-ketocyclopropane products are demonstrated to serve as substrates for SN2, SN2′, and aldehyde cycloaddition reactions.
