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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, 1-(isocyanatomethyl)-2,4-dimethoxy-

O=C=NCc1ccc(cc1OC)OC Request for Quotation
Chemical Name: Benzene, 1-(isocyanatomethyl)-2,4-dimethoxy-
CAS Number: 93489-13-5
Product Number: AG003FTQ(AGN-PC-005BJV)
Synonyms:
MDL No:
Molecular Formula: C10H11NO3
Molecular Weight: 193.1992

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
193.202g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
193.074g/mol
Monoisotopic Mass:
193.074g/mol
Topological Polar Surface Area:
47.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
213
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 1-(Isocyanatomethyl)-2,4-dimethoxybenzene plays a crucial role in chemical synthesis as a versatile building block for the creation of various organic compounds. It is commonly utilized in the production of complex chemicals and pharmaceuticals due to its unique reactivity and structural characteristics.The isocyanatomethyl functional group in the molecule provides a reactive site for forming covalent bonds with other organic molecules, enabling the synthesis of new compounds with specific properties and functionalities. The presence of the dimethoxybenzene moiety further enhances the compound's compatibility with a wide range of reaction conditions and applications in organic chemistry.In chemical synthesis, 1-(Isocyanatomethyl)-2,4-dimethoxybenzene can serve as a key intermediate in the construction of heterocyclic compounds, pharmaceutical intermediates, and specialty chemicals. Its strategic placement within molecular structures allows for the introduction of diverse functional groups and modifications, leading to the development of novel materials and bioactive molecules.With its potential for structural manipulation and reactivity in various synthetic pathways, this compound enables chemists to design and create a wide array of complex organic compounds with tailored properties and applications across different industries.