CAS 613-54-7

2-(Bromoacetyl)naphthalene

Description:

2-(Bromoacetyl)naphthalene is an organic compound characterized by the presence of a naphthalene ring substituted with a bromoacetyl group at the second position. This compound typically appears as a solid, and its molecular structure features both aromatic and aliphatic characteristics due to the naphthalene moiety and the bromoacetyl functional group. It is known for its reactivity, particularly in electrophilic substitution reactions, owing to the electron-rich nature of the naphthalene ring. The bromoacetyl group introduces a polar functional group, which can enhance the compound's solubility in polar solvents. Additionally, 2-(Bromoacetyl)naphthalene can serve as an intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. Safety considerations should be taken into account when handling this compound, as it may pose health risks due to the presence of bromine and its potential reactivity. Proper storage and handling protocols are essential to ensure safety in laboratory environments.

Formula: C₁₂H₉BrO

InChI: InChI=1/C12H9BrO/c13-8-12(14)11-6-5-9-3-1-2-4-10(9)7-11/h1-7H,8H2

InChI key: InChIKey=YHXHHGDUANVQHE-UHFFFAOYSA-N

SMILES: C(CBr)(=O)C1=CC2=C(C=C1)C=CC=C2

Synonyms:

• 2-(2-Bromoacetyl)naphthalene
• 2-(Bromoacetyl)naphthalene
• 2-(α-Bromoacetyl)naphthalene
• 2-Bromo-1-(2-naphthalenyl)ethanone
• 2-Bromo-1-(2-naphthyl)-1-ethanone
• 2-Bromo-1-(2-naphthyl)ethanone
• 2-Bromo-1-(Naphthalen-2-Yl)Ethanone
• 2-Bromo-1-(naphthalen-2-yl)ethan-1-one
• 2-Bromo-2'-acetonaphthone
• 2-Naphthacyl bromide
• 2-Naphthoylmethyl bromide
• 2′-Acetonaphthone, 2-bromo-
• Bromomethyl 2-naphthyl ketone
• Ethanone, 2-bromo-1-(2-naphthalenyl)-
• NSC 36849
• α-Bromo-2-acetonaphthone
• β-Naphthacyl bromide
• ω-Bromo-2-acetonaphthalene
• ω-Bromo-2-acetonaphthone
• alpha-Bromo-2-acetonaphthone
• ω-Bromoaceto-β-naphthone
• TIMTEC-BB SBB000883
• 1-(2-Naphthyl)-2-bromoethanone
• ALPHA-BROMO-2-ACETYL NAPHTHALENE
• SS-NAPHTHACYLBROMIDE
• A-BROMO-2-ACETYLNAPHTHALENE
• Bromomethyl2-naphthylketone,98+%
• 2-Bromo-1-(2-naphtyl)ethane-1-one

2-Bromoacetylnaphthalene

CAS: 613-54-7

Formula: C₁₂H₉BrO

Purity: >98.0%(GC)

Color and Shape: Light yellow to Brown powder to crystal

Molecular weight: 249.11

Ref: 3B-B1259

2-(Bromoacetyl)naphthalene, 98%

CAS: 613-54-7

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Formula: C₁₂H₉BrO

Purity: 98%

Color and Shape: Pale pink to pink to purple to brown, Crystals or powder or crystalline powder

Molecular weight: 249.11

Ref: 02-B23960

2-Bromo-1-(naphthalen-2-yl)ethanone

CAS: 613-54-7

Formula: C₁₂H₉BrO

Purity: 97%

Color and Shape: Solid

Molecular weight: 249.1033

Ref: IN-DA003GM9

2-Bromo-1-(naphthalen-2-yl)ethan-1-one

CAS: 613-54-7

2-Bromo-1-(naphthalen-2-yl)ethan-1-one

Purity: 98%

Molecular weight: 249.107g/mol

Ref: 54-OR74625

2-Bromo-2′-acetonaphthone

CAS: 613-54-7

Formula: C₁₂H₉BrO

Molecular weight: 249.11

Ref: 7W-GL8965

2-bromo-1-(naphthalen-2-yl)ethan-1-one

CAS: 613-54-7

Formula: C₁₂H₉BrO

Purity: 95%

Color and Shape: Solid, Pale yellow - Greyish yellow red powder

Molecular weight: 249.107

Ref: 10-F358274

2-Bromo-2²-acetonaphthone

CAS: 613-54-7

2-Bromo-2²-acetonaphthone (2BA) is a chemical compound belonging to the group of naphthalene derivatives. It has significant inhibitory activities against bacteria, fungi, and protozoans. The 2BA molecule is an antimicrobial agent that binds to fatty acids in the cell membrane and inhibits the synthesis of fatty acids in the mitochondria. This leads to cell death by inhibiting protein synthesis and cell division. 2BA has also been shown to have anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis. The chemical structure of 2BA can be found below:

Formula: C₁₀H₇COCH₂Br

Purity: Min. 95%

Molecular weight: 249.1 g/mol

Ref: 3D-AAA61354