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(4-AMINO-PHENYL)-(4-METHYL-PIPERIDIN-1-YL)-METHANONE, with the chemical formula C14H18N2O, is a synthetic compound characterized by the presence of an amino group, a phenyl group, and a piperidine ring. Its structural features suggest potential applications in pharmaceutical synthesis and organic chemistry, with the amino and phenyl groups indicating possible nucleophilic reactivity or use as ligands in metal-catalyzed reactions. The piperidine ring may also contribute to specific pharmacological effects. Careful handling and disposal are required due to the compound's potential reactivity and toxicity, and further research is needed to explore its full properties and uses.

79868-20-5

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79868-20-5 Usage

Uses

Used in Pharmaceutical Synthesis:
(4-AMINO-PHENYL)-(4-METHYL-PIPERIDIN-1-YL)-METHANONE is used as an intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs. The presence of the amino and phenyl groups allows for further chemical reactions to create a variety of medicinal compounds.
Used in Organic Chemistry:
In the field of organic chemistry, (4-AMINO-PHENYL)-(4-METHYL-PIPERIDIN-1-YL)-METHANONE is used as a reagent or building block for the creation of more complex organic molecules. Its structural components, including the amino and phenyl groups, facilitate its use in various organic reactions.
Used in Research and Development:
(4-AMINO-PHENYL)-(4-METHYL-PIPERIDIN-1-YL)-METHANONE is utilized in research and development settings to explore its chemical properties, reactivity, and potential applications in various chemical and pharmaceutical processes. This includes testing its behavior in different reaction conditions and assessing its toxicity and environmental impact.
Note: Since the provided materials do not specify particular applications or industries for (4-AMINO-PHENYL)-(4-METHYL-PIPERIDIN-1-YL)-METHANONE, the uses listed are general and based on the compound's structural features and potential in the fields of pharmaceuticals and organic chemistry. Further information would be needed to detail specific applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 79868-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,6 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79868-20:
(7*7)+(6*9)+(5*8)+(4*6)+(3*8)+(2*2)+(1*0)=195
195 % 10 = 5
So 79868-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2O/c1-10-6-8-15(9-7-10)13(16)11-2-4-12(14)5-3-11/h2-5,10H,6-9,14H2,1H3

79868-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-aminophenyl)-(4-methylpiperidin-1-yl)methanone

1.2 Other means of identification

Product number -
Other names 1-(4-amino-benzoyl)-4-methyl-piperidine

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:79868-20-5 SDS

79868-20-5Downstream Products

79868-20-5Relevant academic research and scientific papers

2-phenylpyrimidine compounds, preparation method and medical application

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Paragraph 0098; 0099; 0106; 0107; 0108, (2018/06/15)

The invention belongs to the field of medicines and particularly relates to 2-phenylpyrimidine compounds and pharmacologically-acceptable salts thereof and an isotope marker. The invention also discloses a pharmaceutical composition containing the substances and application of the pharmaceutical composition for treating diseases related with protein kinase activity, such as cancer and inflammation. (The formula is shown in the description).

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