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2-Chloro-3-ethylpyrazine is a chemical compound that belongs to the class of pyrazines. Pyrazines are heterocyclic aromatic organic compounds characterized by the presence of two nitrogen atoms in their structure. This particular compound features a chlorine atom at the 2nd position and an ethyl group at the 3rd position. Although detailed information about its physical properties and applications is scarce, it is likely to exhibit aromatic properties due to its molecular structure. The limited availability of data suggests that 2-chloro-3-ethylpyrazine may not be a widely studied or used compound, and it is not listed in regulatory databases, which could indicate that it does not pose significant health or environmental risks. However, it is important to note that the properties and impacts of individual compounds within a chemical class can vary significantly.

63450-95-3

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63450-95-3 Usage

Uses

Due to the limited information available on 2-chloro-3-ethylpyrazine, it is challenging to provide a comprehensive list of its applications. However, based on the general properties of pyrazines, we can infer potential uses in various industries:
Used in Flavor and Fragrance Industry:
2-Chloro-3-ethylpyrazine could be used as a flavoring agent or a fragrance component in the food, beverage, or cosmetic industries. Pyrazines are known for their ability to impart unique aromas and tastes, and 2-CHLORO-3-ETHYLPYRAZINE might contribute to the development of novel scents or flavors.
Used in Chemical Research:
2-Chloro-3-ethylpyrazine may serve as a research compound in academic or industrial laboratories. Its synthesis, properties, and potential reactions could be of interest to chemists studying heterocyclic compounds or exploring new synthetic pathways.
Used in Pharmaceutical Industry:
Although there is no direct evidence of its use in pharmaceuticals, 2-chloro-3-ethylpyrazine could potentially be employed as an intermediate in the synthesis of more complex molecules with medicinal properties. The presence of nitrogen atoms and the chlorine substituent might make it a versatile building block for drug development.
It is important to emphasize that these potential uses are speculative and would require further research and validation to confirm their applicability and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 63450-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,5 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63450-95:
(7*6)+(6*3)+(5*4)+(4*5)+(3*0)+(2*9)+(1*5)=123
123 % 10 = 3
So 63450-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H7ClN2/c1-2-5-6(7)9-4-3-8-5/h3-4H,2H2,1H3

63450-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-3-ethylpyrazine

1.2 Other means of identification

Product number -
Other names 2-CHLORO-3-ETHYLPYRAZINE

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:63450-95-3 SDS

63450-95-3Downstream Products

63450-95-3Relevant academic research and scientific papers

N-heterocyclyl sulphonamide derivatives and their use as endothelin antagonists

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, (2008/06/13)

The invention concerns pharmaceutically useful N-heterocyclyl sulphonamide derivatives, their pharmaceutically acceptable salts, processes for their manufacture, their use for antagonising one or more actions of endothelin in a human or other warm-blooded animal, their use in methods of treatment of diseases or medical conditions in which elevated or abnormal levels of endothelin play a significant causative role.

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