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(1-METHYLENE-ETHYL)PYRAZINE is a synthetic compound derived from the alkylation of the Mannich base, which is obtained by reacting formaldehyde and dimethylamine with ethylpyrazine, followed by the Hoffmann degradation. It is also reported to be found in various food items such as fried chicken, cocoa, roasted peanuts, peanut butter, oat groats, toasted sesame seeds, and malt.

38713-41-6

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38713-41-6 Usage

Uses

Used in Pharmaceutical Industry:
(1-METHYLENE-ETHYL)PYRAZINE is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique chemical structure allows it to be a versatile building block in the development of new drugs.
Used in Flavor and Fragrance Industry:
(1-METHYLENE-ETHYL)PYRAZINE is used as a component in the creation of various flavors and fragrances for [application reason]. Its distinct chemical properties contribute to the development of unique and complex scents in the perfumery and flavoring agents.
Used in Chemical Research:
(1-METHYLENE-ETHYL)PYRAZINE is used as a research compound for [application reason] in various chemical studies. Its synthesis and properties make it an interesting subject for further exploration and potential applications in different fields.
Used in Agrochemical Industry:
(1-METHYLENE-ETHYL)PYRAZINE is used as a component in the development of agrochemicals for [application reason]. Its chemical properties may contribute to the creation of new pesticides, herbicides, or other agricultural products.

Preparation

By alkylation of the Mannich base obtained by reacting formaldehyde and dimethylamine with ethylpyrazine, followed by the Hoffmann degradation

Check Digit Verification of cas no

The CAS Registry Mumber 38713-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38713-41:
(7*3)+(6*8)+(5*7)+(4*1)+(3*3)+(2*4)+(1*1)=126
126 % 10 = 6
So 38713-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2/c1-6(2)7-5-8-3-4-9-7/h3-5H,1H2,2H3

38713-41-6SDS

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 2-prop-1-en-2-ylpyrazine

1.2 Other means of identification

Product number -
Other names 2-Isopropenylpyrazine

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:38713-41-6 SDS

38713-41-6Downstream Products

38713-41-6Relevant academic research and scientific papers

Construction of α-Amino Azines via Thianthrenation-Enabled Photocatalyzed Hydroarylation of Azine-Substituted Enamides with Arenes

Zhang, Yu-Lan,Wang, Gang-Hu,Wu, Yichen,Zhu, Chun-Yin,Wang, Peng

supporting information, p. 8522 - 8526 (2021/11/13)

α-Amino azines are widely found in pharmaceuticals and ligands. Herein, we report a practical method for accessing this class of compounds via photocatalyzed hydroarylation of azine-substituted enamides with the in situ-generated aryl thianthrenium salts as the radical precursor. This reaction features a broad substrate scope, good functional group tolerance, and mild conditions and is suitable for the late-stage installation of α-amino azines in complex structures.

Superacid-catalyzed reactions of olefinic pyrazines: An example of anti-markovnikov addition involving superelectrophiles

Zhang, Yiliang,Briski, Jason,Zhang, Yun,Rendy, Rendy,Klumpp, Douglas A.

, p. 2505 - 2508 (2007/10/03)

(Chemical Equation Presented) Olefinic pyrazines are found to react with benzene in CF3SO3H and give anti-Markovnikov-type addition products. We propose that this is caused by two effects: destabilization of the carbocationic interme

Diarylbutyl octahydropyrazinopyrimidinones and methods of medical treatment using them

-

, (2008/06/13)

2,3,4,7,8,9-Substituted octahydropyrazinopyrimidinones and acid addition salts thereof. A process for the preparation of said compounds. A pharmaceutical composition comprising such a compound and a conventional carrier. A process for the preparation of said composition. Method of medical treatment of human beings and animals using such compounds.

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