4071-15-2 Usage
Uses
Used in Pharmaceutical Research:
2-methyl-3-(piperidin-1-ylmethyl)-1H-indole is used as a potential drug candidate in pharmaceutical research for its unique structural features and the possibility of modulating biological targets. 2-methyl-3-(piperidin-1-ylmethyl)-1H-indole's ability to interact with various receptors or enzymes makes it a promising candidate for the development of new therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-methyl-3-(piperidin-1-ylmethyl)-1H-indole serves as a valuable starting point for the design and synthesis of novel compounds with potential therapeutic applications. Its structural elements can be further modified to optimize pharmacokinetic and pharmacodynamic properties, enhancing its efficacy and safety in treating specific diseases or conditions.
Note: Since the provided materials do not specify particular applications or industries for 2-methyl-3-(piperidin-1-ylmethyl)-1H-indole, the uses listed are general and based on the compound's potential in pharmaceutical research and medicinal chemistry. If there are specific applications or industries where 2-methyl-3-(piperidin-1-ylmethyl)-1H-indole is used, they should be added accordingly.
Check Digit Verification of cas no
The CAS Registry Mumber 4071-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4071-15:
(6*4)+(5*0)+(4*7)+(3*1)+(2*1)+(1*5)=62
62 % 10 = 2
So 4071-15-2 is a valid CAS Registry Number.
4071-15-2Relevant academic research and scientific papers
Mannich Reactions Of Indoles With Dichloromethane And Secondary Amines Under High Pressure
Matsumoto, Kiyoshi,Uchida, Takane,Hashimoto, Shiro,Yonezawa, Yukie,Iida, Hirokazu,et al.
, p. 2215 - 2220 (2007/10/02)
Mannich reactions of indole with dichloromethane and secondary amines gave the corresponding Mannich bases in moderate to good yields, while 2-methylindole afforded only low yields of the Mannich bases.Some limitations were observed in the cases of hinder
