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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-isothiocyanato-1-methoxy-4-methyl-

S=C=Nc1cc(C)ccc1OC Request for Quotation
Chemical Name: Benzene, 2-isothiocyanato-1-methoxy-4-methyl-
CAS Number: 190774-56-2
Product Number: AG002ESC(AGN-PC-0JTLOO)
Synonyms:
MDL No:
Molecular Formula: C9H9NOS
Molecular Weight: 179.2389

Identification/Properties

Computed Properties
Molecular Weight:
179.237g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
179.04g/mol
Monoisotopic Mass:
179.04g/mol
Topological Polar Surface Area:
53.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
189
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


2-METHOXY-5-METHYLPHENYL ISOTHIOCYANATE, also known as MMPI, is a versatile compound commonly used in chemical synthesis as a key building block for various organic reactions. This compound acts as a potent isothiocyanate reagent, allowing for the efficient introduction of the isothiocyanate functional group into organic molecules.MMPI finds wide application in the synthesis of complex organic compounds, particularly in the preparation of bioactive molecules and pharmaceutical intermediates. Its isothiocyanate moiety serves as a valuable reactive handle for the modification of biomolecules and the construction of molecular scaffolds with desired pharmacological properties.Furthermore, 2-METHOXY-5-METHYLPHENYL ISOTHIOCYANATE exhibits excellent reactivity towards nucleophilic species, enabling the selective and regiocontrolled functionalization of diverse substrates. This reactivity profile makes MMPI a valuable tool for the creation of novel chemical entities in drug discovery and medicinal chemistry research.In conclusion, the versatile nature of 2-METHOXY-5-METHYLPHENYL ISOTHIOCYANATE makes it a valuable reagent in chemical synthesis, enabling the efficient construction of complex organic molecules with diverse applications in pharmaceuticals, agrochemicals, and materials science.