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2-methyl-3-(3-phenyl-1H-pyrazol-1-yl)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

197094-10-3

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197094-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197094-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,0,9 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 197094-10:
(8*1)+(7*9)+(6*7)+(5*0)+(4*9)+(3*4)+(2*1)+(1*0)=163
163 % 10 = 3
So 197094-10-3 is a valid CAS Registry Number.

197094-10-3Upstream product

197094-10-3Downstream Products

197094-10-3Relevant academic research and scientific papers

Discovery of Potent N-Ethylurea Pyrazole Derivatives as Dual Inhibitors of Trypanosoma brucei and Trypanosoma cruzi

Varghese, Swapna,Rahmani, Rapha?l,Russell, Stephanie,Deora, Girdhar Singh,Ferrins, Lori,Toynton, Arthur,Jones, Amy,Sykes, Melissa,Kessler, Albane,Eufrásio, Amanda,Cordeiro, Artur Torres,Sherman, Julian,Rodriguez, Ana,Avery, Vicky M.,Piggott, Matthew J.,Baell, Jonathan B.

, p. 278 - 285 (2019)

Trypanosoma brucei (T. brucei) and Trypanosoma cruzi (T. cruzi) are causative agents of parasitic diseases known as human African trypanosomiasis and Chagas disease, respectively. Together, these diseases affect 68 million people around the world. Current

HETEROCYCLIC COMPOUNDS AND USE OF SAME

-

, (2016/01/08)

Novel heterocyclic compounds are provided which display useful efficacy in the treatment of diseases caused by trypanosomatids. Particularly, the compounds of the invention are useful in the treatment of HAT and/or Chagas disease and/or Animal African trypanosomiasis (AAT).

Novel Parham-type Cycloacylations of 1H-Pyrazole-1-alkanoic Acids

Larsen, Scott D.

, p. 1013 - 1014 (2007/10/03)

Exposure of 1H-pyrazole-1-alkanoic acids to two equivalents of n-butyllithium affords the corresponding cyclic ketones via a Parham-type cyclization process. Although yields are modest, this procedure represents a simple and direct intramolecular acylation of a non-nucleophilic pyrazole carbon.

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