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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)-

Benzonitrile, 2-chloro-6-methoxy-

COc1cccc(c1C#N)Cl Request for Quotation
Chemical Name: Benzonitrile, 2-chloro-6-methoxy-
CAS Number: 6575-10-6
Product Number: AG00FAT4(AGN-PC-0JLSZY)
Synonyms:
MDL No:
Molecular Formula: C8H6ClNO
Molecular Weight: 167.5923

Identification/Properties

Computed Properties
Molecular Weight:
167.592g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
167.014g/mol
Monoisotopic Mass:
167.014g/mol
Topological Polar Surface Area:
33A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
174
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-6-methoxybenzonitrile, a key aromatic compound, plays a vital role in chemical synthesis as a versatile building block. It is commonly used as a precursor in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its unique structure and reactivity, this compound is often employed in the synthesis of complex organic molecules through different chemical transformations.In organic synthesis, 2-Chloro-6-methoxybenzonitrile serves as a valuable starting material for the preparation of diverse functionalized compounds. Its nitrile group can undergo various reactions such as nucleophilic substitution, and its aromatic ring can participate in electrophilic aromatic substitution reactions. These properties enable the compound to be used in the construction of biologically active molecules, organic dyes, and other advanced materials. Additionally, the presence of functional groups like methoxy and chlorine offers opportunities for fine-tuning the properties of the final products.Furthermore, 2-Chloro-6-methoxybenzonitrile is known for its compatibility with a wide range of reaction conditions and its ability to facilitate the synthesis of structurally diverse organic compounds. This compound's utility in chemical transformations makes it a valuable tool for organic chemists and researchers working in various fields, including medicinal chemistry, materials science, and agrochemical development.