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1-(3-chloro-4-methoxyphenyl)piperazine is a chemical compound with the molecular formula C11H15ClN2O. It is a derivative of piperazine, an organic compound with a six-membered ring containing two nitrogen atoms. The structure of 1-(3-chloro-4-methoxyphenyl)piperazine features a 3-chloro-4-methoxyphenyl group attached to the piperazine ring, which gives it unique properties. 1-(3-chloro-4-methoxyphenyl)piperazine is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. It is also used in the synthesis of certain psychoactive substances. Due to its chemical structure, it may exhibit various pharmacological effects, and its safety and potential side effects should be carefully considered.

55349-31-0

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55349-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55349-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,4 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55349-31:
(7*5)+(6*5)+(5*3)+(4*4)+(3*9)+(2*3)+(1*1)=130
130 % 10 = 0
So 55349-31-0 is a valid CAS Registry Number.

55349-31-0Relevant academic research and scientific papers

A2B Adenosine Receptor Antagonists with Picomolar Potency

Jiang, Jie,Seel, Catharina Julia,Temirak, Ahmed,Namasivayam, Vigneshwaran,Arridu, Antonella,Schabikowski, Jakub,Baqi, Younis,Hinz, Sonja,Hockemeyer, J?rg,Müller, Christa E.

supporting information, p. 4032 - 4055 (2019/05/06)

The A2B adenosine receptor (A2BAR) was proposed as a novel target for the (immuno)therapy of cancer since A2BAR blockade results in antiproliferative, antiangiogenic, antimetastatic, and immunostimulatory effects. In this study, we explored the structure-activity relationships of xanthin-8-yl-benzenesulfonamides mainly by introducing a variety of linkers and substituents attached to the sulfonamide residue. A new, convergent strategy was established, which facilitated the synthesis of the target compounds. Many of the new compounds exhibited subnanomolar affinity for the A2BAR combined with high selectivity. Functional groups were introduced, which will allow the attachment of dyes and other reporter groups. 8-(4-((4-(4-Bromophenyl)piperazin-1-yl)sulfonyl)phenyl)-1-propylxanthine (34, PSB-1901) was the most potent A2B-antagonist (Ki 0.0835 nM, KB 0.0598 nM, human A2BAR) with >10 000-fold selectivity versus all other AR subtypes. It was similarly potent and selective at the mouse A2BAR, making it a promising tool for preclinical studies. Computational studies predicted halogen bonding to contribute to the outstanding potency of 34.

PHENYLPYRIDINE CARBONYL PIPERAZINE DERIVATIVE

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Page 14, (2008/06/13)

The present invention relates to a compound which is represented by the following general formula and has type 4 phosphodiesterase inhibitory action, and uses and an intermediate compound thereof. (whereinR1, R2: hydrogen, a halogen, a lower alkyl, a lower alkoxy, or the like,R3, R4: hydrogen, a (substituted) lower alkyl, a halogen, or the like,R5: hydrogen, a lower alkyl, a lower alkoxycarbonyl, or the like, andn: 0 or 1).

IMIDAZO[1,2-A]PYRIDINES FOR THE TREATMENT OF CNS AND CARDIAC DISEASES

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, (2008/06/13)

The present invention relates to imidazo[1,2-a]pyridine compounds of formula (1) STR1 which are dopamine D-4 antagonists and useful as anti-psychotic agents.

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