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19808-51-6

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19808-51-6 Usage

Structure

A symmetrical hydrazine derivative with two pyridine rings attached to the hydrazine moiety.

Organic synthesis

Used as a reagent in various chemical reactions.

Pharmaceuticals

Studied for potential applications in the pharmaceutical industry.

Reactivity

Exhibits reactivity towards various chemical reactions, making it a valuable reagent in organic chemistry.

Biological activities

Investigated for potential biological activities, showing promising results in some studies.

Research interest

Of interest to researchers for its potential applications in both chemical and biological fields.

Check Digit Verification of cas no

The CAS Registry Mumber 19808-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,0 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19808-51:
(7*1)+(6*9)+(5*8)+(4*0)+(3*8)+(2*5)+(1*1)=136
136 % 10 = 6
So 19808-51-6 is a valid CAS Registry Number.

19808-51-6Relevant articles and documents

Convenient semihydrogenation of azoarenes to hydrazoarenes using H2

Sahoo, Manoj K.,Sivakumar, Ganesan,Jadhav, Sanjay,Shaikh, Samrin,Balaraman, Ekambaram

supporting information, p. 5289 - 5293 (2021/06/30)

The high atom-economical and eco-benign nature of hydrogenation reactions make them much more superior to conventional reduction and transfer hydrogenation. Herein, a convenient and highly selective hydrogenation reaction of azoarenes using molecular hydrogen to access diverse hydrazoarenes is reported. The present catalytic method is general and operationally simple, and it operates under exceedingly mild conditions (room temperature and 1 atm of hydrogen pressure). The reusability of catalysts used in this method is also successfully demonstrated.

Dehydrogenation of the NH?NH Bond Triggered by Potassium tert-Butoxide in Liquid Ammonia

Wang, Lei,Ishida, Akiko,Hashidoko, Yasuyuki,Hashimoto, Makoto

, p. 870 - 873 (2017/01/14)

A novel strategy for the dehydrogenation of the NH?NH bond is disclosed using potassium tert-butoxide (tBuOK) in liquid ammonia (NH3) under air at room temperature. Its synthetic value is well demonstrated by the highly efficient synthesis of aromatic azo compounds (up to 100 % yield, 3 min), heterocyclic azo compounds, and dehydrazination of phenylhydrazine. The broad application of this strategy and its benefit to chemical biology is proved by a novel, convenient, one-pot synthesis of aliphatic diazirines, which are important photoreactive agents for photoaffinity labeling.

A Novel and Efficient Deoxygenation of Hetero Cyclic N-Oxides Using ZrCl4/NaBH4

Chary, K. Purushothama,Mohan, G. Hari,Iyengar, D. S.

, p. 1339 - 1340 (2007/10/03)

A practical and novel reagent system ZrCl4/NaBH4 is used for the deoxygenation of N-Oxides to amines is described.

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