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9H-beta-carbolin-1-yl(2-methylphenyl)methanone is a complex organic compound with the chemical formula C18H15NO. It is a derivative of beta-carboline, a tricyclic indole alkaloid, and features a 2-methylphenyl group attached to the carbonyl group. 9H-beta-carbolin-1-yl(2-methylphenyl)methanone is known for its potential applications in medicinal chemistry, particularly in the development of drugs targeting the central nervous system. It is characterized by its unique molecular structure, which includes a fused pyrrole and indole ring system, and a methyl group on the phenyl ring. The compound's properties and reactivity are influenced by the presence of the carbonyl group, which can participate in various chemical reactions, such as nucleophilic addition and condensation. Research on compounds like this often focuses on their potential therapeutic effects, including their ability to modulate neurotransmitter activity and their impact on cognitive functions.

6912-99-8

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6912-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6912-99-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6912-99:
(6*6)+(5*9)+(4*1)+(3*2)+(2*9)+(1*9)=118
118 % 10 = 8
So 6912-99-8 is a valid CAS Registry Number.

6912-99-8Downstream Products

6912-99-8Relevant academic research and scientific papers

Synthesis, in vitro anti-inflammatory and cytotoxic evaluation, and mechanism of action studies of 1-benzoyl-β-carboline and 1-benzoyl-3-carboxy-β-carboline derivatives

Yang, Mei-Lin,Kuo, Ping-Chung,Hwang, Tsong-Long,Chiou, Wen-Fei,Qian, Keduo,Lai, Chin-Yu,Lee, Kuo-Hsiung,Wu, Tian-Shung

experimental part, p. 1674 - 1682 (2011/04/16)

In the present study, various 1-substituted and 1,3-disubstituted β-carboline derivatives were synthesized by a modified single-step Pictet-Spengler reaction. The compounds were examined for cytotoxicity and anti-inflammatory activity, as measured by the

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