CAS 6627-78-7

1-Bromo-4-methylnaphthalene

Description:

1-Bromo-4-methylnaphthalene is an organic compound characterized by its structure, which consists of a naphthalene ring substituted with a bromine atom and a methyl group. It is a member of the naphthalene derivatives and is known for its aromatic properties. The presence of the bromine atom introduces a halogen functionality, which can influence its reactivity and solubility. Typically, this compound appears as a solid at room temperature and has a relatively high melting point compared to many other organic compounds. It is generally insoluble in water but soluble in organic solvents such as ethanol and ether. 1-Bromo-4-methylnaphthalene can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it useful in synthetic organic chemistry. Additionally, it may exhibit biological activity, which can be of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₁₁H₉Br

InChI: InChI=1S/C11H9Br/c1-8-6-7-11(12)10-5-3-2-4-9(8)10/h2-7H,1H3

InChI key: InChIKey=IDRVLLRKAAHOBP-UHFFFAOYSA-N

SMILES: BrC=1C2=C(C(C)=CC1)C=CC=C2

Synonyms:

• (5E)-1-(4-bromophenyl)-5-{[(4-fluorophenyl)amino]methylidene}pyrimidine-2,4,6(1H,3H,5H)-trione
• 1-Methyl-4-bromonaphthalene
• 4-Bromo-1-methylnaphthalene
• 4-Methyl-1-bromonaphthalene
• NSC 60231
• Naphthalene, 1-bromo-4-methyl-
• 1-Bromo-4-methylnaphthalene

Naphthalene, 1-bromo-4-methyl-

CAS: 6627-78-7

Formula: C₁₁H₉Br

Purity: 95%

Color and Shape: Liquid

Molecular weight: 221.0932

Ref: IN-DA00FAF3

1-Bromo-4-methylnaphthalene

CAS: 6627-78-7

1-Bromo-4-methylnaphthalene

Purity: 97%

Molecular weight: 221.09g/mol

Ref: 54-OR80779

1-Bromo-4-methylnaphthalene

CAS: 6627-78-7

Formula: C₁₁H₉Br

Purity: >95.0%(GC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 221.10

Ref: 3B-B6185

1-Bromo-4-methylnaphthalene

CAS: 6627-78-7

1-Bromo-4-methylnaphthalene is a brominating agent that reacts with alkenes and alkynes to form bromides. It is a Grignard reagent that can be used for the preparation of chiral derivatives, such as enantiomers, by adding an alkyl halide or other electrophile. This reaction is stereospecific and produces a single diastereomer due to the chiral center present in the compound. 1-Bromo-4-methylnaphthalene has been shown to react with vinyl ethers and form 1,3-diphenylpropane. The addition of this compound to a solution containing an azaarene leads to the formation of a chromatogram that consists of two peaks corresponding to the two possible stereoisomers. 1-Bromo-4-methylnaphthalene also has hydrogen bonding interactions with naphthalene and singlet oxygen,

Formula: CH₃C₁₀H₆Br

Purity: Min. 95%

Molecular weight: 221.09 g/mol

Ref: 3D-FB173013

1-Bromo-4-methylnaphthalene

CAS: 6627-78-7

Formula: C₁₁H₉Br

Purity: 95%

Color and Shape: Liquid

Molecular weight: 221.097

Ref: 10-F225222