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(1-Methyl-[3]piperidyl)-phenyl-methanol is a complex organic compound with the molecular formula C14H21NO. It is a derivative of phenylmethanol, featuring a 1-methyl-3-piperidyl group attached to the phenyl ring. (1-Methyl-[3]piperidyl)-phenyl-methanol is characterized by its unique structure, which combines a phenyl ring with a 3-piperidyl group, a cyclic amine with a methyl substitution. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and chemical intermediates due to its versatile chemical properties. The compound's specific applications may vary, but it is often involved in the creation of compounds with potential therapeutic or industrial uses.

5562-48-1

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5562-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5562-48-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5562-48:
(6*5)+(5*5)+(4*6)+(3*2)+(2*4)+(1*8)=101
101 % 10 = 1
So 5562-48-1 is a valid CAS Registry Number.

5562-48-1Downstream Products

5562-48-1Relevant academic research and scientific papers

Structure-activity relationships of diphenylpiperazine N-type calcium channel inhibitors

Pajouhesh, Hassan,Feng, Zhong-Ping,Ding, Yanbing,Zhang, Lingyun,Pajouhesh, Hossein,Morrison, Jerrie-Lynn,Belardetti, Francesco,Tringham, Elizabeth,Simonson, Eric,Vanderah, Todd W.,Porreca, Frank,Zamponi, Gerald W.,Mitscher, Lester A.,Snutch, Terrance P.

scheme or table, p. 1378 - 1383 (2010/07/06)

A novel series of compounds derived from the previously reported N-type calcium channel blocker NP118809 (1-(4-benzhydrylpiperazin-1-yl)-3,3-diphenylpropan-1-one) is described. Extensive SAR studies resulted in compounds with IC50 values in the range of 10-150 nM and selectivity over the L-type channels up to nearly 1200-fold. Orally administered compounds 5 and 21 exhibited both anti-allodynic and anti-hyperalgesic activity in the spinal nerve ligation model of neuropathic pain.

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