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5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine is a complex organic compound with the molecular formula C14H15F3N3O2S. It features a pyrazolo[4,3-c]pyridine core, which is a fused ring system consisting of a pyrazole and a pyridine. The compound is characterized by a methanesulfonyl group (-SO2CH3) at the 5-position and a 4-trifluoromethyl-phenyl group attached at the 3-position. The tetrahydro prefix indicates that the compound has four hydrogen atoms added across the molecule, specifically in the 4,5,6,7 positions, which implies a reduction in the degree of unsaturation compared to a fully unsaturated analog. This chemical structure is significant in medicinal chemistry, as it can be found in certain drug candidates or intermediates, potentially due to its ability to interact with biological targets through its unique arrangement of functional groups.

400797-90-2

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400797-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 400797-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,7,9 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 400797-90:
(8*4)+(7*0)+(6*0)+(5*7)+(4*9)+(3*7)+(2*9)+(1*0)=142
142 % 10 = 2
So 400797-90-2 is a valid CAS Registry Number.

400797-90-2Relevant academic research and scientific papers

An Efficient Synthesis of Substituted Pyrazoles from One-Pot Reaction of Ketones, Aldehydes, and Hydrazine Monohydrochloride

Lellek, Vit,Chen, Cheng-Yi,Yang, Wanggui,Liu, Jie,Ji, Xuebao,Faessler, Roger

supporting information, p. 1071 - 1075 (2018/02/26)

An efficient, one-pot and metal-free process for the preparation of 3,5-disubstituted and 3,4,5-trisubstituted pyrazoles on multi-gram scale was developed. One-pot condensation of ketones, aldehydes and hydrazine monohydrochloride readily formed pyrazoline intermediates under mild conditions. Oxidation of pyrazolines, in situ, employing bromine afforded a wide variety of pyrazoles. The methodology offers a fast, and often chromatography-free protocol for the synthesis of 3,4,5-substituted pyrazoles in good to excellent yields. Alternatively, a more benign oxidation protocol affords 3,5-disubstituted or 3,4,5-trisubstituted pyrazoles by simply heating pyrazolines in DMSO under oxygen.

PROCESS FOR THE PREPARATION OF CATHEPSIN S INHIBITORS

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Page/Page column 130, (2011/02/24)

Inhibitors of Cathepsin S enzyme and their synthetic processes.

Method for treating allergies using substituted pyrazoles

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, (2008/06/13)

A method for treating an allergic condition, including an atopic allergic condition, using substituted pyrazoles.

Method for treating allergies using substituted pyrazoles

-

, (2008/06/13)

A method for treating an allergic condition, including an atopic allergic condition, using substituted pyrazoles.

Method for treating allergies using substituted pyrazoles

-

, (2008/06/13)

A method for treating an allergic condition, including an atopic allergic condition, using substituted pyrazoles.

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