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2,5-dimethyl-3-(4-fluorophenyl)-1-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole is a complex organic compound characterized by its unique molecular structure that features a dimethyl group, a fluorophenyl group, a methyl-tetrahydropyridinyl group, and an indole ring. As a derivative of the heterocyclic indole, which is prevalent in many natural products, this chemical may hold potential pharmaceutical applications due to its distinctive structural and property attributes. However, further research is essential to ascertain its specific uses and potential impacts.

141307-02-0

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141307-02-0 Usage

Uses

Given the provided materials, there are no explicit uses listed for 2,5-dimethyl-3-(4-fluorophenyl)-1-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole. 2,5-dimethyl-3-(4-fluorophenyl)-1-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole is described as having potential pharmaceutical applications due to its unique structure and properties, but without specific details on its applications or the reasons for its use in any particular industry. Further research is necessary to explore and confirm its practical applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 141307-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,0 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141307-02:
(8*1)+(7*4)+(6*1)+(5*3)+(4*0)+(3*7)+(2*0)+(1*2)=80
80 % 10 = 0
So 141307-02-0 is a valid CAS Registry Number.

141307-02-0Downstream Products

141307-02-0Relevant academic research and scientific papers

Selective, Centrally Acting Serotonin 5-HT2 Antagonists. 2. Substituted 3-(4-Fluorophenyl)-1H-indoles

Andersen, Kim,Perregaard, Jens,Arnt, Joern,Nielsen, Joern Bay,Begtrup, Mikael

, p. 4823 - 4831 (2007/10/02)

A series of 3-(4-fluorophenyl)-1H-indoles substituted in the 1-position with 4-piperidinyl, 1,2,3,6-tetrahydro-4-pyridinyl, and 4-piperazinyl was synthesized. By variation of the substituents in the benzene part of the indole nucleus in 1-2-4-3-(4-fluo

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