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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)-

Benzene, (2-methoxyethyl)-

COCCc1ccccc1 Request for Quotation
Chemical Name: Benzene, (2-methoxyethyl)-
CAS Number: 3558-60-9
Product Number: AG003BNQ(AGN-PC-0CZN9P)
Synonyms:
MDL No:
Molecular Formula: C9H12O
Molecular Weight: 136.1910

Identification/Properties

Properties
BP:
172.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Refractive Index:
1.4980 to 1.5000
Computed Properties
Molecular Weight:
136.194g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
136.089g/mol
Monoisotopic Mass:
136.089g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
74.8
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:
H227-H303+H313-H316
Precautionary Statements:
P210-P280-P312-P332+P313-P370+P378-P403+P235-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2-Methoxyethyl)benzene, also known as veratrole, serves as a valuable compound in chemical synthesis due to its unique properties and versatile applications. This aromatic ether is commonly used as a solvent in various chemical reactions and as a building block in the synthesis of complex organic molecules. In particular, (2-Methoxyethyl)benzene is utilized in the production of pharmaceuticals, agrochemicals, and materials such as polymers and fragrances. Its ability to undergo functional group transformations, such as halogenation and nitration, makes it an essential intermediate in the synthesis of diverse chemical compounds. Furthermore, the presence of the methoxy group provides additional reactivity and selectivity in many reactions, leading to efficient and high-yielding processes. With its importance in organic synthesis, (2-Methoxyethyl)benzene plays a crucial role in advancing research and development across various industries.