Introduction：Basic information about CAS 2142-70-3|2'-Iodoacetophenone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | 2'-Iodoacetophenone |
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| CAS Number | 2142-70-3 | Molecular Weight | 246.04500 |
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| Density | 1.72 g/mL at 25 °C(lit.) | Boiling Point | 139-140°C 12mm |
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| Molecular Formula | C8H7IO | Melting Point | / |
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| MSDS | / | Flash Point | 218 °F |
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Names
| Name | 1-(2-iodophenyl)ethanone |
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| Synonym | More Synonyms |
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Chemical & Physical Properties
| Density | 1.72 g/mL at 25 °C(lit.) |
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| Boiling Point | 139-140°C 12mm |
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| Molecular Formula | C8H7IO |
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| Molecular Weight | 246.04500 |
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| Flash Point | 218 °F |
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| Exact Mass | 245.95400 |
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| PSA | 17.07000 |
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| LogP | 2.49380 |
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| Vapour Pressure | 0.00779mmHg at 25°C |
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| Index of Refraction | n20/D 1.618(lit.) |
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| InChIKey | XDXCBCXNCQGZPG-UHFFFAOYSA-N |
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| SMILES | CC(=O)c1ccccc1I |
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Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US) |
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| Hazard Codes | C: Corrosive; |
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| Risk Phrases | R36/38 |
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| Safety Phrases | S26-S36 |
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| RIDADR | NONH for all modes of transport |
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| WGK Germany | 3 |
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| HS Code | 2914700090 |
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Customs
| 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% |
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Articles3
More Articles
| Trapping evidence for the thermal cyclization of di-(o-acetylphenyl)acetylene to 3,3'-dimethyl-1,1'-biisobenzofuran. Beilstein J. Org. Chem. 1(1) , 18, (2005) The reaction of di-(o-acetylphenyl)acetylene (1) with excess dimethyl acetylenedicarboxylate (DMAD) produced bis-DMAD adducts meso-3 and rac-3. This transformation is suggested to involve thermal rear... | |
| Cobalt-catalyzed regioselective carbocyclization reaction of o-iodophenyl ketones and aldehydes with alkynes, acrylates, and acrylonitrile: a facile route to indenols and indenes. J. Org. Chem. 69(14) , 4781-7, (2004) An efficient cobalt-catalyzed carbocylization for the synthesis of indenols and indenes and a new method for reductive decyanation are described. 2-Iodophenyl ketones and aldehydes 1a-g undergo carboc... | |
| Cobalt-Catalyzed Carbocyclization of o-Iodobenzaldehydes and o-Iodophenylketones with Alkynes. Chang KJ, et al. Org. Lett. 5(21) , 3963-3966, (2003)
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Synonyms
| 1-(2-iodophenyl)ethan-1-one |
| 2-IC6H4COMe |
| 2′-Iodoacetophenone |
| MFCD00094998 |
| 2-Ac-C6H4-I |
| 2‘-Iodoacetophenone |
| o-Iodoacetophenone |
| ortho-iodoacetophenone |
| 2'-Iodoacetophenone |
| 2-Iodoacetophenone |
| 2'-IODO-1,1':3',1''-TERPHENYL |
| o-acetyl-iodobenzene |
| 1-acetyl-2-iodobenzene |
| Acetophenone,o-iodo |
| 1-(2-Iodophenyl)ethanone |
