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4-Piperidinecarbonitrile, 4-[(3-methoxyphenyl)amino]-1-(phenylmethyl)-, also known as 4-[(3-methoxyphenyl)amino]-1-(phenylmethyl)piperidine-4-carbonitrile, is a complex organic compound with the molecular formula C20H22N2O. It is a derivative of piperidine, a heterocyclic amine, and features a carbonitrile group, a phenylmethyl group, and a 3-methoxyphenyl group attached to the piperidine ring. 4-Piperidinecarbonitrile, 4-[(3-methoxyphenyl)amino]-1-(phenylmethyl)- is characterized by its unique chemical structure, which may have potential applications in the synthesis of pharmaceuticals or other organic compounds. Due to its specific functional groups and structural features, it is important to handle 4-Piperidinecarbonitrile, 4-[(3-methoxyphenyl)amino]-1-(phenylmethyl)- with care, as it may have specific reactivity or properties that are not yet fully understood.

974-71-0

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974-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 974-71-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 974-71:
(5*9)+(4*7)+(3*4)+(2*7)+(1*1)=100
100 % 10 = 0
So 974-71-0 is a valid CAS Registry Number.

974-71-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-(3-methoxyanilino)piperidine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-Benzyl-4-cyano-4-m-methoxyanilinopiperidin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:974-71-0 SDS

974-71-0Downstream Products

974-71-0Relevant academic research and scientific papers

Nonpeptide small molecule agonist and antagonist original leads for neuropeptide FF1 and FF2 receptors

Journigan, V. Blair,Mésangeau, Christophe,Vyas, Neha,Eans, Shainnel O.,Cutler, Stephen J.,McLaughlin, Jay P.,Mollereau, Catherine,McCurdy, Christopher R.

, p. 8903 - 8927 (2015/03/14)

Neuropeptide FF1 and FF2 receptors (NPFF1-R and NPFF2-R), and their endogenous ligand NPFF, are one of only several systems responsible for mediating opioid-induced hyperalgesia, tolerance, and dependence. Currently, no small molecules displaying good affinity or selectivity for either subtype have been reported, to decipher the role of NPFF2-R as it relates to opioid-mediated analgesia, for further exploration of NPFF1-R, or for medication development for either subtype. We report the first nonpeptide small molecule scaffold for NPFF1,2-R, the guanidino-piperidines, and SAR studies resulting in the discovery of a NPFF1 agonist (7b, Ki = 487 ± 117 nM), a NPFF1 antagonist (46, Ki = 81 ± 17 nM), and a NPFF2 partial antagonist (53a, Ki = 30 ± 5 nM), which serve as leads for the development of pharmacological probes and potential therapeutic agents. Testing of 46 alone was without effect in the mouse 48 °C warm-water tail-withdrawal test, but pretreatment with 46 prevented NPFF-induced hyperalgesia.

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