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Ethanone, 1-(1-methyl-1H-1,2,3-triazol-5-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

194209-18-2

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194209-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194209-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,2,0 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 194209-18:
(8*1)+(7*9)+(6*4)+(5*2)+(4*0)+(3*9)+(2*1)+(1*8)=142
142 % 10 = 2
So 194209-18-2 is a valid CAS Registry Number.

194209-18-2Downstream Products

194209-18-2Relevant academic research and scientific papers

TETRAHYDRONAPHTHYRIDINE DERIVATIVES AS mGluR2-NEGATIVE ALLOSTERIC MODULATORS, COMPOSITIONS, AND THEIR USE

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Page/Page column 51; 52, (2016/03/22)

Provided are quinoline carboxamide and quinoline carbonitrile compounds of formula (I) or a pharmaceutically acceptable salt thereof, wherein R 1, R 2, L, X 1, X 2, and X 3, are as defined herein. The compounds of the invention, and pharmaceutically acceptable salts thereof, and pharmaceutical compositions comprising them, are useful as non-competitive mGluR2 antagonists, or mGluR2 negative allosteric modulators (NAMs), and may be useful in methods of treating a person in need thereof for diseases or disorders in which the mGluR2-NAM receptor plays a causative role, such as Alzheimer's disease, cognitive impairment, schizophrenia and other mood disorders, pain disorders and sleep disorders.

Alkylation and acylation of the 1,2,3,triazole ring

Ohta, Shunsaku,Kawasaki, Ikuo,Uemura, Takahiro,Yamashita, Masayuki,Yoshioka, Tomomichi,Yamaguchi, Satoshi

, p. 1140 - 1145 (2007/10/03)

Trimethylsilylation of 1,2,3-triazole regioselectively proceeded to give 2-trimethylsilyl-2H-1,2,3-triazole, which was treated with primary alkyl halides in the presence of tetrabutylammonium fluoride to give 1-alkyl-1H- 1,2,3-triazoles as a Sole product 1-Methyl-5-substituted 1H-1,2,3-triazoles were prepared by alkylation of 5-lithio-1-methyl-1H-1,2,3-triazole, and 1- methyl-4-substituted 1H-1,2,3-triazoles were obtained by alkylation of 4- lithio-1-methyl-5-phenylthio-1H-1,2,3-triazole followed by reductive desulfurization.

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