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93865-37-3

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93865-37-3 Usage

Molecular Weight

250.35 g/mol The relative molecular mass of this compound, based on the atomic weights of its constituent elements, is approximately 250.35 grams per mole.

Chemical Structure

The structure of 1-oxo-3-phenyl-1-piperidin-1-ylpropan-2-amine consists of a piperidine ring (a five-membered nitrogen-containing ring) with a substituted phenyl group (a benzene ring with attached substituents) and a ketone functional group (a carbonyl group bonded to two carbon atoms).

Piperidine Derivative

This compound is a derivative of piperidine, which is a common structural motif found in many pharmaceutical drugs and natural alkaloids.

Substituents

The phenyl group in this compound is substituted with a ketone functional group, which is responsible for its reuptake inhibitory activity.

Neurotransmitter Reuptake Inhibitor

1-oxo-3-phenyl-1-piperidin-1-ylpropan-2-amine has been reported to act as a neurotransmitter reuptake inhibitor, which means it can potentially increase the levels of certain neurotransmitters in the brain by blocking their reabsorption into the presynaptic neuron.

Central Nervous System Effects

Due to its reuptake inhibitory activity, this compound may have an impact on the central nervous system, potentially affecting mood, cognition, and other neurological functions.

Therapeutic Potential

1-oxo-3-phenyl-1-piperidin-1-ylpropan-2-amine is commonly used in pharmaceutical research as a potential therapeutic agent for various conditions, although its specific uses and effectiveness are still being investigated.

Psychoactive Substances

This compound has been identified as a common structural motif in certain psychoactive substances, which may contribute to its potential effects on the central nervous system.

Ongoing Research

Further research is needed to fully understand the properties, effects, and potential applications of 1-oxo-3-phenyl-1-piperidin-1-ylpropan-2-amine, as its specific uses and mechanisms of action have not yet been fully elucidated.

Check Digit Verification of cas no

The CAS Registry Mumber 93865-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,8,6 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93865-37:
(7*9)+(6*3)+(5*8)+(4*6)+(3*5)+(2*3)+(1*7)=173
173 % 10 = 3
So 93865-37-3 is a valid CAS Registry Number.

93865-37-3SDS

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 2-Amino-3-phenyl-1-(1-piperidinyl)-1-propanone

1.2 Other means of identification

Product number -
Other names 2-Anilino-3-phenoxazinon

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:93865-37-3 SDS

93865-37-3Relevant articles and documents

Highly Enantioselective Hydrogenation of Amides via Dynamic Kinetic Resolution Under Low Pressure and Room Temperature

Rasu, Loorthuraja,John, Jeremy M.,Stephenson, Elanna,Endean, Riley,Kalapugama, Suneth,Clément, Roxanne,Bergens, Steven H.

supporting information, p. 3065 - 3071 (2017/03/11)

High-throughput screening and lab-scale optimization were combined to develop the catalytic system trans-RuCl2((S,S)-skewphos)((R,R)-dpen), 2-PrONa, and 2-PrOH. This system hydrogenates functionalized α-phenoxy and related amides at room temperature under 4 atm H2 pressure to give chiral alcohols with up to 99% yield and in greater than 99% enantiomeric excess via dynamic kinetic resolution.

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