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1-Phenyl-3-piperidin-1-ylthiourea is an organic compound with the chemical formula C12H18N3S. It is a derivative of thiourea, featuring a phenyl group attached to the thiourea molecule and a piperidin-1-yl group at the 3-position. 1-phenyl-3-piperidin-1-ylthiourea is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a building block for the synthesis of various biologically active molecules. Its structure provides a unique combination of aromatic and aliphatic characteristics, which can influence its reactivity and interactions with other molecules. The compound is typically synthesized through the reaction of phenyl isothiocyanate with piperidine, and it is an important intermediate in the preparation of more complex thiourea-based compounds.

5446-55-9

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5446-55-9 Usage

Structure

Contains a thiourea derivative, a piperidine ring, and a phenyl group

Pharmacological properties

Activity as a nicotinic acetylcholine receptor antagonist

Potential use

Drug development for central nervous system disorders

Cancer cell growth inhibition

Has been investigated for its potential role in inhibiting the growth of cancer cells

Chemical tool

Can be used as a chemical tool in biological research

Diverse applications

Potential for diverse applications in the fields of pharmacology and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 5446-55-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5446-55:
(6*5)+(5*4)+(4*4)+(3*6)+(2*5)+(1*5)=99
99 % 10 = 9
So 5446-55-9 is a valid CAS Registry Number.

5446-55-9SDS

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-phenyl-3-piperidin-1-ylthiourea

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-piperidin-1-yl-thiourea

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:5446-55-9 SDS

5446-55-9Downstream Products

5446-55-9Relevant academic research and scientific papers

Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors

Taha, Muhammad,Ismail, Nor Hadiani,Jamil, Waqas,Khan, Khalid Mohammed,Salar, Uzma,Kashif, Syed Muhammad,Rahim, Fazal,Latif, Yawar

, p. 3166 - 3173 (2015/08/03)

Thiourea analogs 1-20 were synthesized and evaluated for their in vitro β-glucuronidase inhibitory potential. The compounds 9 (0.86 ± 0.01 μM), 6 (1.24 ± 0.01 μM), 16 (1.64 ± 0.02 μM) and 15 (2.12 ± 0.02 μM) showed potent activity. Other analogs 1-5, 7, 8

Pharmaceutical composition comprising N-aryl N' morpholino/piperidino thiocarbamide derivatives for treating and preventing diabetes, diabetic complications, insulin resistance and insulin resistance syndrome

-

Page/Page column 3, (2008/06/13)

Disclosed is a medicament comprising N-aryl N′ morpholino/piperidino thiocarbamide derivatives represented by the following formula 1 for preventing and treating diabetes, diabetic complications, insulin resistance and insulin resistance syndrome, and can be used in drugs, foods, and beverages inducing an effect of preventing and treating diabetes, diabetic complications, insulin resistance and insulin resistance syndrome of modern people who suffer from the increasing development of diabetes resulting from environmental factors, such as intake of westernized foods, obesity, and so on: wherein, X is O or C, and R represents 4-chlorophenyl, 2-methylphenyl, 3-methoxypheny, 3-methylphenyl, or phenyl group.

Preparation and properties of antitubercular 1-piperidino-3-arylthioureas [1]

Hearn, Michael J.,Webster, Eleanor R.,Cynamon, Michael H.

, p. 1225 - 1229 (2007/10/03)

1-Piperidino-3-arylthioureas, of interest in the investigation of novel heterocyclic structures for their antitubercular activity, may be conveniently prepared in good yield and purity by the reaction of 1-aminopiperidine with aryl isothiocyanates in etha

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