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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)-

1,2-Dibromo-4-methoxy-3,5,6-trimethylbenzene

COc1c(C)c(C)c(c(c1C)Br)Br Request for Quotation
Chemical Name: 1,2-Dibromo-4-methoxy-3,5,6-trimethylbenzene
CAS Number: 1359986-20-1
Product Number: AG00A122(AGN-PC-0WAH1M)
Synonyms:
MDL No:
Molecular Formula: C10H12Br2O
Molecular Weight: 308.0097

Identification/Properties

Computed Properties
Molecular Weight:
308.013g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
307.923g/mol
Monoisotopic Mass:
305.925g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
13
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,2-Dibromo-4-methoxy-3,5,6-trimethylbenzene is a versatile chemical compound widely utilized in chemical synthesis processes. Due to its unique molecular structure, this compound serves as a valuable building block in the creation of various complex organic molecules.In chemical synthesis, 1,2-Dibromo-4-methoxy-3,5,6-trimethylbenzene can be employed as a key reagent for the introduction of functional groups such as bromine, methoxy, and methyl onto target molecules. Its ability to undergo selective reactions makes it a valuable tool for organic chemists seeking to modify and fine-tune the properties of their synthesized compounds.Furthermore, the presence of bromine and methoxy groups in 1,2-Dibromo-4-methoxy-3,5,6-trimethylbenzene imparts unique reactivity and properties to the resulting molecules. This compound can act as a powerful intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials with specific desired characteristics.Overall, the strategic incorporation of 1,2-Dibromo-4-methoxy-3,5,6-trimethylbenzene in chemical synthesis enables researchers to access a diverse array of functionalized organic compounds with tailored properties for various industrial applications.