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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Pyrazine, 2-chloro-3-ethyl-

CCc1nccnc1Cl Request for Quotation
Chemical Name: Pyrazine, 2-chloro-3-ethyl-
CAS Number: 63450-95-3
Product Number: AG00E8RX(AGN-PC-0JLIWG)
Synonyms:
MDL No:
Molecular Formula: C6H7ClN2
Molecular Weight: 142.5862

Identification/Properties

Properties
BP:
184.6°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
142.586g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
142.03g/mol
Monoisotopic Mass:
142.03g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
87.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-3-ethylpyrazine is a versatile chemical compound that finds extensive application in chemical synthesis processes. As a halogenated pyrazine derivative, it serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its specific chemical structure and reactivity make it a crucial intermediate in the synthesis of complex organic molecules.One of the key applications of 2-Chloro-3-ethylpyrazine is in the pharmaceutical industry, where it is used as a precursor in the production of novel drug candidates. By incorporating this compound into the molecular structure of pharmaceutical compounds, chemists can modify the properties of the resulting drug, such as its bioavailability, stability, or therapeutic activity. This makes 2-Chloro-3-ethylpyrazine an essential tool in drug discovery and development efforts.In addition to pharmaceuticals, 2-Chloro-3-ethylpyrazine is also utilized in the synthesis of agrochemicals, such as pesticides and herbicides. By harnessing its chemical properties, researchers can create effective pest control agents that help farmers protect their crops from insects, weeds, and other harmful organisms. The role of this compound in agrochemical synthesis underscores its importance in enhancing agricultural productivity and food security.Furthermore, 2-Chloro-3-ethylpyrazine is employed in the creation of fine chemicals, which are high-value substances used in various industries, including cosmetics, flavors, and fragrances. Its unique structure and reactivity make it a valuable component in the production of specialty chemicals that impart specific characteristics to consumer products. This highlights the versatility and significance of 2-Chloro-3-ethylpyrazine in enabling the development of diverse chemical compounds for commercial applications.