Phenacyl Bromide structure
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Common Name | Phenacyl Bromide | ||
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CAS Number | 2142-69-0 | Molecular Weight | 199.05 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | 249.0±23.0 °C at 760 mmHg | |
Molecular Formula | C8H7BrO | Melting Point | °C | |
MSDS | Chinese USA | Flash Point | 86.6±9.9 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of Phenacyl Bromide2'-Bromoacetophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 2'-Bromoacetophenone |
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Synonym | More Synonyms |
Description | 2'-Bromoacetophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog | |
In Vitro | 2-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。 |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 249.0±23.0 °C at 760 mmHg |
Melting Point | °C |
Molecular Formula | C8H7BrO |
Molecular Weight | 199.05 |
Flash Point | 86.6±9.9 °C |
Exact Mass | 197.968018 |
PSA | 17.07000 |
LogP | 2.28 |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.554 |
Storage condition | -20°C |
Water Solubility | PRACTICALLY INSOLUBLE |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
Packaging Group | I; II; III |
Hazard Class | 6.1 |
HS Code | 29147090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2914700090 |
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Summary | HS: 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% |
Enantioselective alkynylation of aromatic ketones catalyzed by chiral camphorsulfonamide ligands.
Angew. Chem. Int. Ed. Engl. 42(41) , 5057-8, (2003)
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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)
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Palladium-catalysed convenient synthesis of 3-methyleneisoindolin-1-ones. Cho CS, et al.
Synth. Commun. 32(!2) , 1821-27, (2002)
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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 |