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105283-71-4

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105283-71-4 Usage

General Description

4-(4-Fluoro-benzenesulfonyl)-piperidine hydrochloride is a chemical compound consisting of a piperidine ring with a fluoro-benzenesulfonyl group attached to it in the para position. It is in the form of a hydrochloride salt, making it more stable and soluble in water. 4-(4-Fluoro-benzenesulfonyl)-piperidine hydrochloride has potential applications in medicinal chemistry, particularly as a building block in the synthesis of pharmaceuticals. It may also have uses in organic synthesis as a reagent or intermediate in the production of other compounds. However, its specific properties and uses would depend on further research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 105283-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,8 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105283-71:
(8*1)+(7*0)+(6*5)+(5*2)+(4*8)+(3*3)+(2*7)+(1*1)=104
104 % 10 = 4
So 105283-71-4 is a valid CAS Registry Number.

105283-71-4Downstream Products

105283-71-4Relevant articles and documents

TETRAHYDROPYRIDOPYRAZINES MODULATORS OF GPR6

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Paragraph 0162, (2015/07/02)

The present invention provides compounds of formula I: which are useful as modulators of GPR6, pharmaceutical compositions thereof, methods for treatment of conditions associated with GPR6, processes for making the compounds and intermediates thereof.

PYRAZINES MODULATORS OF GPR6

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Paragraph 0140; 0143, (2015/09/22)

The present invention provides compounds of formula (I): which are useful as modulators of GPR6, pharmaceutical compositions thereof, methods for treatment of conditions associated with GPR6, processes for making the compounds and intermediates thereof.

Discovery of a piperidine-4-carboxamide CCR5 antagonist (TAK-220) with highly potent anti-HIV-1 activity

Imamura, Shinichi,Ichikawa, Takashi,Nishikawa, Youichi,Kanzaki, Naoyuki,Takashima, Katsunori,Niwa, Shinichi,Iizawa, Yuji,Baba, Masanori,Sugihara, Yoshihiro

, p. 2784 - 2793 (2007/10/03)

We incorporated various polar groups into previously described piperidine-4-carboxamide CCR5 antagonists to improve their metabolic stability in human hepatic microsomes. Introducing a carbamoyl group into the phenyl ring of the 4-benzylpiperidine moiety

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