6971-57-9 Usage
Uses
Used in Scientific Research:
6-METHYL-2-PICOLYL-METHYLAMINE is used as a research chemical for various scientific applications, including the study of its chemical properties, reactivity, and potential interactions with other compounds.
Used in Chemical Synthesis:
In the chemical synthesis industry, 6-METHYL-2-PICOLYL-METHYLAMINE is used as a building block or intermediate in the production of more complex organic compounds. Its unique structure allows it to be incorporated into a wide range of molecules, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Coordination Chemistry:
6-METHYL-2-PICOLYL-METHYLAMINE is used as a ligand in coordination chemistry, where it can form coordination complexes with metal ions. These complexes have potential applications in various fields, such as catalysis, materials science, and supramolecular chemistry.
Used in Pharmaceutical Development:
Due to its reactivity and unique structure, 6-METHYL-2-PICOLYL-METHYLAMINE can be used in the development of new pharmaceuticals. It may serve as a starting material or intermediate in the synthesis of drug candidates with potential therapeutic applications.
Used in Agrochemicals:
In the agrochemical industry, 6-METHYL-2-PICOLYL-METHYLAMINE can be used in the synthesis of active ingredients for pesticides, herbicides, and other crop protection products. Its unique properties may contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Specialty Chemicals:
6-METHYL-2-PICOLYL-METHYLAMINE can be utilized in the production of specialty chemicals for various applications, such as dyes, fragrances, and other fine chemicals. Its versatility and reactivity make it a valuable component in the synthesis of these high-value products.
Check Digit Verification of cas no
The CAS Registry Mumber 6971-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6971-57:
(6*6)+(5*9)+(4*7)+(3*1)+(2*5)+(1*7)=129
129 % 10 = 9
So 6971-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-7-4-3-5-8(10-7)6-9-2/h3-5,9H,6H2,1-2H3
6971-57-9Relevant academic research and scientific papers
Base-Promoted Tandem Synthesis of 2-Azaaryl Tetrahydroquinolines
Chen, Shuguang,Yang, Langxuan,Shang, Yongjia,Mao, Jianyou,Walsh, Patrick J.
supporting information, p. 1594 - 1599 (2021/03/08)
A novel method to synthesize 2-azaaryl tetrahydroquinolines by the base-promoted tandem reaction of azaaryl methyl amines and styrene derivatives is reported (over 30 examples, yields up to 95%). Mechanistic probe experiments demonstrate that the deprotonation of the benzylic C-H bond and the addition to the styrene vinyl group proceeds via the SNAr mechanism.
Selective synthesis of mono- and di-methylated amines using methanol and sodium azide as C1 and N1 sources
Chakrabarti, Kaushik,Mishra, Anju,Panja, Dibyajyoti,Paul, Bhaskar,Kundu, Sabuj
supporting information, p. 3339 - 3345 (2018/07/29)
A Ru(ii) complex mediated synthesis of various N,N-dimethyl and N-monomethyl amines from organic azides using methanol as a methylating agent is reported. This methodology was successfully applied for a one-pot reaction of bromide derivatives and sodium azide in methanol. Notably, by controlling the reaction time several N-monomethylated and N,N-dimethylated amines were synthesized selectively. The practical applicability of this tandem process was revealed by preparative scale reactions with different organic azides and synthesis of an anti-vertigo drug betahistine. Several kinetic experiments and DFT studies were carried out to understand the mechanism of this transformation.
POTENTIAL CNS ACTIVE 1-ARYL-2-AMINO-1-ETHANOL DERIVATIVES
Zara-Kaczian, Erzsebet,Deak, Gyula,Gyoergy, Lajos
, p. 441 - 454 (2007/10/02)
New N-(picolyl)-2-(methylamino)-1-aryl-1-ethanols (I) and their O-acyl derivatives (II) were synthesized.Their dopaminomimetic and antidepressant biological activities were examined and compared with the activities of N-(2-aminobenzyl)-2-(methylamino)-1-aryl-1-ethanols (III).It was established that in the reaction of N- methylamine (2) and styryl oxide, the two directions of the splitting of the epoxide ring give rise to two different products that were isolated and identified in the form of their O-acetyl derivatives (13 and 15, respectively).
