CAS 27060-75-9

4-Bromo-3-methylanisole

Description:

4-Bromo-3-methylanisole, with the CAS number 27060-75-9, is an organic compound that belongs to the class of aromatic ethers. It features a methoxy group (-OCH3) and a bromine atom attached to a benzene ring, specifically at the 4 and 3 positions, respectively. This compound is characterized by its molecular formula, which reflects the presence of bromine and a methyl group, contributing to its unique chemical properties. It typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. 4-Bromo-3-methylanisole is known for its applications in organic synthesis and as an intermediate in the production of various chemical compounds. Its reactivity is influenced by the electron-withdrawing nature of the bromine atom and the electron-donating properties of the methoxy group, which can affect its behavior in electrophilic aromatic substitution reactions. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry and research. Safety precautions should be taken when handling this compound due to its potential toxicity and environmental impact.

Formula: C₈H₉BrO

InChI: InChI=1S/C8H9BrO/c1-6-5-7(10-2)3-4-8(6)9/h3-5H,1-2H3

InChI key: InChIKey=BLZNSXFQRKVFRP-UHFFFAOYSA-N

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

Synonyms:

• 1-Brom-4-methoxy-2-methylbenzol
• 1-Bromo-2-methyl-4-methoxybenzene
• 1-Bromo-4-methoxy-2-methylbenzene
• 2-Bromo-5-methoxytoluene
• 3-Methyl-4-bromoanisole
• 4-Bromo-3-methylphenyl methyl ether
• Anisole, 4-bromo-3-methyl-
• Benzene, 1-bromo-4-methoxy-2-methyl-
• 4-Bromo-3-methylanisole

4-Bromo-3-methylanisole, 97%

CAS: 27060-75-9

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₈H₉BrO

Purity: 97%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 201.06

Ref: 02-A12318

Benzene, 1-bromo-4-methoxy-2-methyl-

CAS: 27060-75-9

Formula: C₈H₉BrO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 201.0605

Ref: IN-DA00I54Y

2-Bromo-5-methoxytoluene, min. 98%

CAS: 27060-75-9

Formula: C₈H₉BrO

Purity: min. 98%

Color and Shape: Clear, colorless liquid

Molecular weight: 201.06

Ref: 08-06-0059

2-Bromo-5-methoxytoluene

CAS: 27060-75-9

Formula: C₈H₉BrO

Purity: >97.0%(GC)

Color and Shape: White or Colorless to Almost white or Almost colorless powder to lump to clear liquid

Molecular weight: 201.06

Ref: 3B-B1782

4-Bromo-3-methylanisole

CAS: 27060-75-9

4-Bromo-3-methylanisole

Formula: C₈H₉BrO

Purity: 97%

Color and Shape: clear. almost colourless liquid

Molecular weight: 201.06g/mol

Ref: 54-OR4933

2-Bromo-5-methoxytoluene

CAS: 27060-75-9

2-Bromo-5-methoxytoluene is a synthetic organic compound that is used as a chemical intermediate for cellulose derivatives. It is generated by the Friedel-Crafts reaction of bromine with toluene in the presence of aluminum chloride. 2-Bromo-5-methoxytoluene has been shown to react with cellulose derivatives and other hydrogen bond acceptors. This reaction is followed by protonation, which yields a chromophore that changes color from yellow to orange. The mechanism of this reaction can be explained by an acid catalysis mechanism, which begins with protonation of the carbonyl group (C=O) and formyl group (HC=O) groups. This causes the formation of an enolate ion, which reacts with a protonated carbonyl group to yield a formyl cation and an enolate ion. The formyl cation then reacts with another proton

Formula: C₈H₉OBr

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 201.06 g/mol

Ref: 3D-FB64878

2-Bromo-5-methoxytoluene

CAS: 27060-75-9

Formula: C₈H₉BrO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 201.063

Ref: 10-F018291