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3-[4-(4-Chloro-benzyl)-piperazin-1-yl]-propan-1-ol is a complex organic compound with the molecular formula C16H22ClNO2. It features a propane-1-ol backbone, which is a three-carbon chain with a hydroxyl group at one end. Attached to this chain is a piperazine ring, which is a heterocyclic compound with two nitrogen atoms in a six-membered ring. The piperazine ring is further substituted with a 4-chlorobenzyl group, which is a benzyl group (a phenylmethyl group) with a chlorine atom attached to the para position of the benzene ring. 3-[4-(4-Chloro-benzyl)-piperazin-1-yl]-propan-1-ol is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its chemical structure and properties make it a versatile building block for the development of new therapeutic agents.

79837-34-6

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79837-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79837-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,3 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79837-34:
(7*7)+(6*9)+(5*8)+(4*3)+(3*7)+(2*3)+(1*4)=186
186 % 10 = 6
So 79837-34-6 is a valid CAS Registry Number.

79837-34-6Relevant academic research and scientific papers

Studies on 1,2,3-Triazoles. 13. (Piperazinylalkoxy)benzopyrano-1,2,3-triazol-9(1H)-ones with Combined H1-Antihistamine and Mast Cell Stabilizing Properties

Buckle, Derek R.,Rockell, Caroline J. M.,Smith, Harry,Spicer, Barbara A.

, p. 2262 - 2267 (2007/10/02)

Several N-benzylpiperazino derivatives of benzopyrano-1,2,3-triazol-9(1H)-one and its 5-methyl homologue have been prepared and evaluated for H1-antihistamine activity on guinea pig ileum.The most potent compounds were also evaluated for their ability to stabilize mast cells in the rat passive peritoneal anaphylaxis (PPA) system and were shown to inhibit histamine-release at concentrations below those required to inhibit extravasation, suggesting that this might be relevant to their antianaphylactic activity in this system.The compound tested with the most triazol-9(1H)-one, 28, which had a pA2 of 9.1 against histamine on guinea pig ileum, comparable to that of mepyramine, and inhibited histamine release in the rat PPA system with an IC50 value of 5.4E-6 M.

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