CAS 51699-89-9

1,3-Dibromo-2-methoxy-5-methylbenzene

Description:

1,3-Dibromo-2-methoxy-5-methylbenzene, also known by its CAS number 51699-89-9, is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with two bromine atoms, a methoxy group (-OCH3), and a methyl group (-CH3). The presence of the bromine atoms introduces significant reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and cross-coupling reactions. The methoxy group contributes to the compound's solubility in organic solvents and can influence its electronic properties, enhancing its reactivity in electrophilic aromatic substitution reactions. The methyl group, being a sterically bulky substituent, can affect the compound's overall steric hindrance and reactivity. This compound is typically used in synthetic organic chemistry and may serve as an intermediate in the synthesis of more complex molecules. Its physical properties, such as melting point, boiling point, and solubility, can vary based on the specific conditions and purity of the sample.

Formula: C₈H₈Br₂O

InChI: InChI=1S/C8H8Br2O/c1-5-3-6(9)8(11-2)7(10)4-5/h3-4H,1-2H3

InChI key: InChIKey=IHOLQYYMMKYVLH-UHFFFAOYSA-N

SMILES: O(C)C1=C(Br)C=C(C)C=C1Br

Synonyms:

• 1,3-Dibromo-2-Methoxy-5-Methylbenzene
• 2,6-Dibromo-4-methylmethoxybenzene
• Benzene, 1,3-dibromo-2-methoxy-5-methyl-
• 2,6-Dibromo-4-methylanisole

2,6-Dibromo-4-methylanisole

CAS: 51699-89-9

Formula: C₈H₈Br₂O

Purity: 97%

Color and Shape: Liquid

Molecular weight: 279.9565

Ref: IN-DA00DKQU

2,6-Dibromo-4-methylanisole

CAS: 51699-89-9

2,6-Dibromo-4-methylanisole

Formula: C₈H₈Br₂O

Purity: 98%

Color and Shape: clear. colourless liquid

Molecular weight: 279.96g/mol

Ref: 54-OR900776

1,3-Dibromo-2-methoxy-5-methylbenzene

CAS: 51699-89-9

Purity: 97%

Molecular weight: 279.9590149

Ref: 10-F693522

2,6-Dibromo-4-Methylanisole

CAS: 51699-89-9

2,6-Dibromo-4-Methylanisole is a methoxylated compound that can be used to produce enantiopure compounds. It is an intermediate in the synthesis of 2,4-dichlorobenzophenone and 2,6-dichloro-4-(methylthio)phenol. The reactivity of this compound is due to its ability to form hydrogen bonding interactions with transition metal ions such as nickel(II). Methylation by 2,6-dibromo-4-methylanisole can also be achieved using other methylating agents such as methyl iodide or dimethyl sulfate. This compound has a polydentate structure which means that it can coordinate with multiple metal ions at once. Steric interactions are also important for the reactivity of this compound. Debromination is an important reaction in the synthesis of 2,6-dibromo-4-(methylth

Formula: C₈H₈Br₂O

Purity: Min. 95%

Molecular weight: 279.96 g/mol

Ref: 3D-BCA69989