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2-[(6-CHLORO-3-PYRIDAZINYL)AMINO]-1-ETHANOL, also known as clopidol, is a chemical compound that serves as an effective anticoccidial agent in poultry farming. It is recognized for its ability to disrupt the growth and development of protozoan parasites known as coccidia, which are responsible for causing coccidiosis, a highly contagious disease in poultry.
Used in Poultry Industry:
2-[(6-CHLORO-3-PYRIDAZINYL)AMINO]-1-ETHANOL is used as an anticoccidial agent for the prevention and control of coccidiosis in poultry. It is administered in the feed or water of poultry to maintain the health and productivity of the flocks, thereby helping to prevent serious illness and economic losses caused by the disease.

51947-89-8

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51947-89-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51947-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,4 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51947-89:
(7*5)+(6*1)+(5*9)+(4*4)+(3*7)+(2*8)+(1*9)=148
148 % 10 = 8
So 51947-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H8ClN3O/c7-5-1-2-6(10-9-5)8-3-4-11/h1-2,11H,3-4H2,(H,8,10)

51947-89-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H61432)  2-(6-Chloro-3-pyridazinylamino)ethanol, 97%   

  • 51947-89-8

  • 250mg

  • 375.0CNY

  • Detail
  • Alfa Aesar

  • (H61432)  2-(6-Chloro-3-pyridazinylamino)ethanol, 97%   

  • 51947-89-8

  • 1g

  • 1117.0CNY

  • Detail
  • Alfa Aesar

  • (H61432)  2-(6-Chloro-3-pyridazinylamino)ethanol, 97%   

  • 51947-89-8

  • 5g

  • 4486.0CNY

  • Detail

51947-89-8Relevant academic research and scientific papers

IMIDAZOPYRIDINE DERIVATIVES AS INHIBITORS OF RECEPTOR TYROSINE KINASES

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Page/Page column 136, (2010/01/07)

The invention relates to new bicyclic heterocyclic derivative compounds, to pharmaceutical compositions comprising said compounds and to the use of said compounds in the treatment of diseases, e.g. cancer.

Efficient preparation of imidazo[1,2-b]pyridazines under Swern oxidative conditions

Raboisson, Pierre,Mekonnen, Belew,Peet, Norton P.

, p. 2919 - 2921 (2007/10/03)

An efficient synthesis of new imidazo[1,2-b]pyridazine derivatives was effected by treating 3,6-dichloropyridazine with various 2-hydroxyethylamines following by imidazole ring formation under Swern oxidative conditions. Some mechanistic aspects of the cyclization step are discussed.

Quinoxaline studies. 23. Potential antimalarials. Substituted 5,8-dimethoxy-6-[N-(omega-dimethylaminoalkyl)amino]quinoxalines were prepared: the first series with identical 2,3-substituents H, CH3, C6H5, C6H4-4-Cl, and CH2C6H5; and the second with identical styryl groups CH=CHC6H5, CH=CHC6H4-4-Cl, CH=CHC6H3-3,4-Cl2, CH=CHC6H4-4-F, CH=CHC6H4-4-CF3, and CH=CHC6H4-4-NO2. None of the substances

Pifferi,Parravicini,Carpi,Dorigotti

, p. 741 - 746 (2007/10/04)

3-Hydrazinopyridazines substituted in position 6 with a primary amine, secondary amine, or an alkoxy group were synthesized and screened for antihypertensive activity. In general, the 6-dialklamino derivatives are the most active; the (2-hydroxypropyl)methylamino chain provides the best combination of high antihypertensive activity and toxicity.

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