CAS 2142-69-0|Phenacyl Bromide

Introduction:Basic information about CAS 2142-69-0|Phenacyl Bromide, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NamePhenacyl Bromide
CAS Number2142-69-0Molecular Weight199.05
Density1.5±0.1 g/cm3Boiling Point249.0±23.0 °C at 760 mmHg
Molecular FormulaC8H7BrOMelting Point°C
MSDSChineseUSAFlash Point86.6±9.9 °C
Symbol
GHS07
Signal WordWarning

Names

Name2'-Bromoacetophenone
SynonymMore Synonyms

Phenacyl Bromide BiologicalActivity

Description2'-Bromoacetophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related CatalogResearch Areas >>OthersSignaling Pathways >>Others >>Others
In Vitro2-bromoacetophenone 用于胞嘧啶部分的选择性衍生化,用于通过反相高效液相色谱法和分光光度计检测法测定整体 DNA 甲基化。

Chemical & Physical Properties

Density1.5±0.1 g/cm3
Boiling Point249.0±23.0 °C at 760 mmHg
Melting Point°C
Molecular FormulaC8H7BrO
Molecular Weight199.05
Flash Point86.6±9.9 °C
Exact Mass197.968018
PSA17.07000
LogP2.28
Vapour Pressure0.0±0.5 mmHg at 25°C
Index of Refraction1.554
InChIKeyPIMNFNXBTGPCIL-UHFFFAOYSA-N
SMILESCC(=O)c1ccccc1Br
Storage condition-20°C
Water SolubilityPRACTICALLY INSOLUBLE

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective EquipmentEyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard CodesXi:Irritant;
Risk PhrasesR36/37/38
Safety PhrasesS26-S36-S37/39
RIDADRNONH for all modes of transport
WGK Germany3
Packaging GroupI; II; III
Hazard Class6.1
HS Code29147090

Customs

HS Code2914700090
SummaryHS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

Articles3

More Articles
Enantioselective alkynylation of aromatic ketones catalyzed by chiral camphorsulfonamide ligands.

Angew. Chem. Int. Ed. Engl. 42(41) , 5057-8, (2003)

Non-Condensed Trifluoromethylated 5, 5-Bicycles: Synthesis of 2-[3-Alkyl (phenyl)-1H-pyrazol-1-yl]-4-phenyl-5-alkylthiazole and-4, 5, 6, 7-tetrahydrobenzothiazole Systems. Bonacorso HG, et al.

Synthesis 2002(08) , 1079-83, (3003)

Palladium-catalysed convenient synthesis of 3-methyleneisoindolin-1-ones. Cho CS, et al.

Synth. Commun. 32(!2) , 1821-27, (2002)

Synonyms

ortho-bromoacetophenone
Phenacyl Bromide
2‘-Bromoacetophenone
2-Bromoacetophenone
EINECS 218-398-1
2′-Bromoacetophenone
Ethanone, 1- (2-bromophenyl)-
o-Bromoacetophenone
Ethanone, 1-(2-bromophenyl)-
o-MeOC-Ph-Br
1-(2-Bromophenyl)ethanone
2-Bromo-1-phenylethanone
2'-Bromoacetophenone
Acetophenone, o-bromo-
o-bromoacetophnones
MFCD00000067
α-Bromoacetophenone
o-MeOC-C6H4-Br
Acetophenone, 2'-bromo-
acetophenone, 2-bromo-
2'-BromoActophenone
Ethanone, 2-bromo-1-phenyl-
1-ACETYL-2-BROMOBENZENE
2-Bromo-1-Phenylethan-1-One
1-Bromo-2-acetylbenzene
Acetophenone,o-bromo
2-Acetyl-1-bromobenzene
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