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2-(Piperidinomethyl)acrylonitrile, with the molecular formula C9H14N2, is a chemical compound that is a derivative of acrylonitrile, featuring a piperidinomethyl group. It is known for its high reactivity and is utilized in the synthesis of pharmaceuticals and fine chemicals, making it a valuable component in organic synthesis and pharmaceutical research. However, due to its toxicity and potential health risks, it is classified as a hazardous substance that requires careful handling.

27315-95-3

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27315-95-3 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(Piperidinomethyl)acrylonitrile is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex molecular structures that can exhibit therapeutic properties.
Used in Fine Chemicals Production:
In the production of fine chemicals, 2-(Piperidinomethyl)acrylonitrile serves as a reactive building block, enabling the creation of specialty compounds with specific applications in various industries.
Used in Organic Synthesis Research:
2-(Piperidinomethyl)acrylonitrile is utilized as a research compound in organic synthesis, where its reactivity is explored for developing new synthetic pathways and understanding reaction mechanisms.
Used in Chemical Education and Training:
Due to its reactivity and the potential hazards associated with its use, 2-(Piperidinomethyl)acrylonitrile can be employed in educational settings to train chemists and researchers on the safe handling and application of hazardous chemicals in a laboratory environment.

Check Digit Verification of cas no

The CAS Registry Mumber 27315-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,1 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27315-95:
(7*2)+(6*7)+(5*3)+(4*1)+(3*5)+(2*9)+(1*5)=113
113 % 10 = 3
So 27315-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2/c1-9(7-10)8-11-5-3-2-4-6-11/h1-6,8H2

27315-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(piperidin-1-ylmethyl)prop-2-enenitrile

1.2 Other means of identification

Product number -
Other names 2-piperidin-1-ylmethyl-acrylonitrile

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:27315-95-3 SDS

27315-95-3Relevant academic research and scientific papers

A new access to 2-(chloromethyl)acrylonitrile

Krawczyk

, p. 3357 - 3362 (1995)

An efficient method for the preparation of 2-(chloromethyl)acrylonitrile (7) is reported. The Mannich reaction of cyanoacetic acid with paraformaldehyde and morpholine afforded the allylic amine 6a which was converted into the chloride 7 on treatment with isobutyl chloroformate at room temperature.

2-(Substitutedpiperidylmethyl)propene and propane nitriles

-

, (2008/06/13)

Antimicrobial agents suitable for use in aqueous systems for their preservation against biodeterioration include substitutedpiperidinomethyl-propenenitriles and propanenitriles. The unsaturated compounds are prepared by reaction of a suitable piperidine w

Treatment of pain, fever, and inflammation with compositions containing 2-(substitutedpiperidinomethyl)propane and propene nitriles

-

, (2008/06/13)

A method of treating pain, fever, and inflammation and pharmaceutical compositions for use therein, wherein the active ingredient comprises a compound of the formula: STR1 wherein A and R1 represent various substituents.

3-Pyrazolidinone derivatives

-

, (2008/06/13)

3-Pyrazolidinone compounds having a solubility of at least 12 grams/liter in an aqueous medium of pH 9 of the formula: STR1 wherein R is a mononuclear phenyl group having substituents in the 3, 4, or 5 positions with a total of no more than 4 non-metallic

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