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(S)-2-Ethylpiperidine is a chemical compound featuring a piperidine ring with an ethyl substituent attached to the second carbon atom. It is recognized for its versatile reactivity, making it a valuable building block in the synthesis of a wide range of pharmaceuticals and organic compounds. Additionally, it finds applications in the production of agrochemicals, dyes, and perfumes, and is characterized by its liquid state and faint amine odor. Due to its potential hazards, it is crucial to handle (S)-2-Ethylpiperidine with proper care and safety protocols.

34272-40-7

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34272-40-7 Usage

Uses

Used in Pharmaceutical Industry:
(S)-2-Ethylpiperidine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to enhance the reactivity and functionality of the compounds being developed. It contributes to the creation of new drugs with improved therapeutic properties.
Used in Agrochemical Production:
(S)-2-Ethylpiperidine is used as a building block in the production of agrochemicals, where it plays a role in the development of pesticides and other agricultural chemicals that help protect crops and enhance yield.
Used in Dye and Perfume Industries:
(S)-2-Ethylpiperidine is used as a raw material in the formulation of dyes and perfumes, contributing to the creation of vibrant colors and distinct scents in various consumer products.
Used in Organic Compound Synthesis:
(S)-2-Ethylpiperidine is used as a versatile reagent in the synthesis of organic compounds, facilitating the development of new chemical entities with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 34272-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,7 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34272-40:
(7*3)+(6*4)+(5*2)+(4*7)+(3*2)+(2*4)+(1*0)=97
97 % 10 = 7
So 34272-40-7 is a valid CAS Registry Number.

34272-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-Ethylpiperidine

1.2 Other means of identification

Product number -
Other names (S)-2-Aethyl-piperidin

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:34272-40-7 SDS

34272-40-7Relevant academic research and scientific papers

Stereoelectronic basis for the kinetic resolution of n-heterocycles with chiral acylating reagents

Hsieh, Sheng-Ying,Wanner, Benedikt,Wheeler, Philip,Beauchemin, Andre M.,Rovis, Tomislav,Bode, Jeffrey W.

supporting information, p. 7228 - 7231 (2014/06/23)

The kinetic resolution of N-heterocycles with chiral acylating agents reveals a previously unrecognized stereoelectronic effect in amine acylation. Combined with a new achiral hydroxamate, this effect makes possible the resolution of various N-heterocycles by using easily prepared reagents. A transition-state model to rationalize the stereochemical outcome of this kinetic resolution is also proposed.

Expanded substrate scope and catalyst optimization for the catalytic kinetic resolution of N-heterocycles

Hsieh, Sheng-Ying,Binanzer, Michael,Kreituss, Imants,Bode, Jeffrey W.

supporting information, p. 8892 - 8894 (2012/11/07)

The scope, reactivity, and selectivity of the chiral hydroxamic acid-catalyzed kinetic resolution of chiral amines are improved by a new catalyst structure and a more environmentally friendly reaction protocol. In addition to increasing selectivity across all substrates, these conditions make possible the resolution of N-heterocycles containing lactams or other basic functional groups that can inhibit the catalyst.

THERAPEUTIC COMBINATIONS COMPRISING A SELECTIVE ESTROGEN RECEPTOR MODULATOR AND A SELECTIVE ANDROGEN RECEPTOR MODULATOR

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Page/Page column 19, (2010/10/20)

This invention relates to a pharmaceutical combination of a selective estrogen receptor modulator (SERM) and a selective androgen receptor modulator (SARM). Particularly, this invention relates to a pharmaceutical composition comprising cis-6-phenyl-5-(4-(2-pyrrolidin-1-yl-ethoxy)-phenyl)-5,6,7,8-tetrahydronapthalene-2-ol, or a pharmaceutically acceptable salt thereof; and a selective androgen receptor modulator. This invention also relates to methods of treatment using the pharmaceutical composition comprising cis-6-phenyl-5-(4-(2-pyrrolidin-1-yl-ethoxy)-phenyl)-5,6,7,8-tetrahydronapthalene-2-ol, or a pharmaceutically acceptable salt thereof; and a selective androgen receptor modulator. Particularly, this invention is directed to methods to prevent and/or restore age-related decline in muscle mass and strength, treat a wasting disease, treat a condition that prevents with low bone mass, increase muscle mass, increase lean body mass, decrease fat body mass, treat bone fracture and muscle damage and treat female sexual dysfunction in mammals, including humans.

BENZONITRILE DERIVATIVES TO TREAT MUSCULOSKELETAL FRAILTY

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, (2010/02/14)

This invention relates to novel amino substituted benzonitrile derivatives and to pharmaceutical compositions containing the novel amino substituted benzonitrile derivatives. This invention also relates to methods of treatment using amino substituted benzonitrile derivatives to prevent and/or restore age-related decline in muscle mass and strength, treat a wasting disease, treat a condition that prevents with low bone mass, increase muscle mass, increase lean body mass, decrease fat body mass, and treat bone fracture and muscle damage in mammals, including humans.

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