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(3-AMINO-PHENYL)-PIPERIDIN-1-YL-METHANONE is a chemical compound with the molecular formula C13H16N2O. It is a piperidine derivative, which means it contains a six-membered heterocyclic ring with a nitrogen atom. (3-AMINO-PHENYL)-PIPERIDIN-1-YL-METHANONE also features a phenyl group and an amino group, as well as a ketone functional group. Its structure and properties make it a versatile intermediate in organic chemistry, with potential applications in drug discovery and development.

77201-13-9

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77201-13-9 Usage

Uses

Used in Pharmaceutical Industry:
(3-AMINO-PHENYL)-PIPERIDIN-1-YL-METHANONE is used as a building block in the synthesis of various pharmaceutical drugs and organic compounds. Its unique structure and functional groups make it a valuable intermediate for the development of new medications and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 77201-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,0 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77201-13:
(7*7)+(6*7)+(5*2)+(4*0)+(3*1)+(2*1)+(1*3)=109
109 % 10 = 9
So 77201-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O/c13-11-6-4-5-10(9-11)12(15)14-7-2-1-3-8-14/h4-6,9H,1-3,7-8,13H2

77201-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-aminophenyl)-piperidin-1-ylmethanone

1.2 Other means of identification

Product number -
Other names 3-aminophenyl piperidyl ketone

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:77201-13-9 SDS

77201-13-9Upstream product

77201-13-9Relevant academic research and scientific papers

METHODS OF CONTROLLING CROP PESTS USING AROMATIC AMIDE INSECT REPELLENTS, METHODS OF MAKING AROMATIC AMIDE INSECT REPELLENTS, AND NOVEL AROMATIC AMIDE INSECT REPELLENTS

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Paragraph 0070, (2022/03/18)

Methods of protecting fruit crops from flying insect pests and of repelling flying insects using aromatic amide compounds are disclosed. The methods apply the compounds to various surfaces, such as the fruit crops, the ground or structures adjacent to the fruit crops, or an object, article, human skin or animal. The compounds have the formula RxC6Hy—C(═O)—N(Cy), where RxC6Hy is a substituted phenyl group, each R group is independently C1-C6 alkyl, substituted C1-C4 alkyl, (substituted) C6-C10 aryl, C1-C4 alkoxy, C6-C10 aryloxy, halogen, nitro, cyano, cyanate, isocyanate, nitroso, C1-C4 alkylthio, phenylthio, (halogen-substituted) C1-C4 alkylsulfonyl, phenylsulfonyl, tolylsulfonyl, amino, mono- or di-C1-C4 alkylamino, diphenylamino, di-C1-C4 alkylamido, formyl, C2-C7 acyl, or C1-C6 alkoxycarbonyl; x is an integer of 1 to 5; x+y=5; Cy is a C2-C8 (substituted) alkadiyl, a C4-C6 (substituted) alkenediyl, or a (substituted) diyl of the formula —(CH2CH2)—O—(CH2CH2)—, —(CH2CH2)—NR′—(CH2CH2)— or —(CH2CH2)—S—(CH2CH2)— that, along with the amide N atom, forms a non-aromatic cyclic group; and R′ is C1-C6 alkyl, substituted C1-C4 alkyl, (substituted) C6-C10 aryl, or (substituted) benzyl.

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