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4-benzyl-1-dodecyl-1H-1,2,3-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1376606-01-7

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1376606-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1376606-01-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,6,6,0 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1376606-01:
(9*1)+(8*3)+(7*7)+(6*6)+(5*6)+(4*0)+(3*6)+(2*0)+(1*1)=167
167 % 10 = 7
So 1376606-01-7 is a valid CAS Registry Number.

1376606-01-7Relevant academic research and scientific papers

Synthesis of α-Keto-1,2,3-triazoles through copper iodide catalyzed oxygenation

Nawratil, Swantje,Grypioti, Maria,Menendez, Christophe,Mallet-Ladeira, Sonia,Lherbet, Christian,Baltas, Michel

, p. 654 - 659 (2014/02/14)

Benzyltriazoles have been catalytically oxidized by using CuI and tert-butyl hydroperoxide to yield phenyl(1H-1,2,3-triazol-4-yl)methanone derivatives in good yields at room temperature. Benzyltriazoles have been catalytically oxidized by using CuI and tert-butyl hydroperoxide to yield phenyl(1H-1,2,3-triazol-4-yl)methanone derivatives in good yields at room temperature. Copyright

Synthesis of α-keto-1,2,3-triazoles through copper iodide catalyzed oxygenation

Nawratil, Swantje,Grypioti, Maria,Menendez, Christophe,Mallet-Ladeira, Sonia,Lherbet, Christian,Baltas, Michel

, p. 654 - 659 (2015/10/05)

Benzyltriazoles have been catalytically oxidized by using CuI and tert-butyl hydroperoxide to yield phenyl(1H-1,2,3-triazol-4-yl)methanone derivatives in good yields at room temperature.

Chemical synthesis and biological evaluation of triazole derivatives as inhibitors of InhA and antituberculosis agents

Menendez, Christophe,Chollet, Aurélien,Rodriguez, Frédéric,Inard, Cyril,Pasca, Maria Rosalia,Lherbet, Christian,Baltas, Michel

, p. 275 - 283 (2012/07/30)

A series of triazoles have been prepared and evaluated as inhibitors of InhA as well as inhibitors of Mycobacterium tuberculosis H37R v. Several of these new compounds possess a good activity against InhA, particularly compounds 17 and 18 for which molecular docking has been performed. Concerning their activities against M. tuberculosis H 37RV strain, two of them, 3 and 12, were found to be good inhibitors with MIC values of 0.50 and 0.25 μg/mL, respectively. Particularly, compound 12 presenting the best MIC value of all compounds tested (0.6 μM) is totally inactive against InhA.

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