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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-iodo-2,3-dimethoxy-

COc1c(OC)cccc1I Request for Quotation
Chemical Name: Benzene, 1-iodo-2,3-dimethoxy-
CAS Number: 25245-33-4
Product Number: AG003EFG(AGN-PC-0KKN5X)
Synonyms:
MDL No:
Molecular Formula: C8H9IO2
Molecular Weight: 264.0603

Identification/Properties

Properties
MP:
43-45 °C
BP:
274.5 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
264.062g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
263.965g/mol
Monoisotopic Mass:
263.965g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Iodo-2,3-dimethoxybenzene is a versatile chemical reagent commonly used in organic synthesis reactions. This compound serves as a key building block in the creation of various complex organic molecules due to its unique chemical properties. In chemical synthesis, 1-Iodo-2,3-dimethoxybenzene can participate in a range of important reactions such as halogenation, coupling reactions, and nucleophilic substitution. By utilizing this compound in synthesis processes, chemists are able to introduce the specific iodo and dimethoxy functional groups into target molecules, allowing for the modification and enhancement of desired chemical properties. The application of 1-Iodo-2,3-dimethoxybenzene in chemical synthesis enables researchers to access a diverse array of structurally intricate organic compounds with tailored functionalities, making it an indispensable tool in the field of organic chemistry.