| Identification | More | [Name]
2'-Bromoacetophenone | [CAS]
2142-69-0 | [Synonyms]
1-(2-BROMOMPHENYL)ETHANONE
1-(2-BROMOPHENYL)ETHANONE
1-ACETYL-2-BROMOBENZENE
2'-BROMOACETOPHENONE
2-BROMOACETOPHENONE
AKOS BBS-00004325
ETHANONE, 1-(2-BROMOPHENYL)-
O-BROMOACETOPHENONE
O-BROMOPHENYL METHYL KETONE
Acetophenone, o-bromo-
o-bromoacetophnones
2'-Bromoacetophenone 1-(2-Bromophenyl)ethanone o-Bromoacetophenone
2-Bromoacetophenone,~97%
2'-BromoActophenone
2'-Bromoacetophenone
1-Acetyl-2-bromobenzene,o-Bromoacetophenone
1-(2-Bromophenyl)ethan-1-one
1-Bromo-2-acetylbenzene
2-Acetyl-1-bromobenzene
Methyl (2-bromophenyl) ketone | [EINECS(EC#)]
218-398-1 | [Molecular Formula]
C8H7BrO | [MDL Number]
MFCD00000067 | [Molecular Weight]
199.04 | [MOL File]
2142-69-0.mol |
| Chemical Properties | Back Directory | [Appearance]
Clear pale yellow to orange liquid | [Melting point ]
°C | [Boiling point ]
116-117 °C (12 mmHg)
| [density ]
1.476 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.568(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Liquid | [color ]
Clear pale yellow to orange | [Specific Gravity]
1.476 | [Water Solubility ]
PRACTICALLY INSOLUBLE | [BRN ]
1931534 | [InChIKey]
PIMNFNXBTGPCIL-UHFFFAOYSA-N | [CAS DataBase Reference]
2142-69-0(CAS DataBase Reference) | [NIST Chemistry Reference]
Ethanone, 1-(2-bromophenyl)-(2142-69-0) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HS Code ]
29147090 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear pale yellow to orange liquid | [Uses]
2-bromoacetophenone is employed in the selective derivatization of cytosine moieties for the determination of global DNA methylation by reversed phase high performance liquid chromatography with spectrofluorimetric detection. | [General Description]
2′-Bromoacetophenone (2-Bromoacetophenone) undergoes enantioselective addition reaction with phenylacetylene catalyzed by chiral camphorsulfonamide. It reacts with aliphatic primary amines in the presence of palladium catalyst to afford 3-methyleneisoindolin-1-ones. |
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