2-Chlorophenol
From Self-sufficiency
| 2-Chlorophenol[1][2][3][4] | |
|---|---|
| 2-Chlorophenol | |
| Other names 2-Hydroxychlorobenzene, o-Chlorophenol | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 95-57-8 
|
| ChemSpider | 6975 |
| SMILES | Script error: No such module "collapsible list". |
| InChI | Script error: No such module "collapsible list". |
| InChI key | ISPYQTSUDJAMAB-UHFFFAOYAM |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C6H5ClO |
| Molar mass | 128.56 g/mol |
| Appearance | Light amber, liquid |
| Density | 1.2634 g/cm3 at 20 °C |
| Melting point |
9.4 °C |
| Boiling point |
174.9 °C |
| Solubility in water | 20 g/L at 20 °C |
| Solubility | soluble in ethanol, diethyl ether, benzene |
| Vapor pressure | 0.308 kPa |
| Acidity (pKa) | 8.56 |
| style="background: #F8EABA; text-align: center;" colspan="2" | Thermochemistry | |
| Specific heat capacity, C | 1.468 J·g-1·K-1 |
| style="background: #F8EABA; text-align: center;" colspan="2" | Hazards | |
| MSDS | External MSDS |
| Main hazards | Corrosive - causes burns |
| Flash point | 64°C |
| Autoignition temperature |
550 °C |
| style="background: #F8EABA; text-align: center;" colspan="2" | Related compounds | |
| Related aromatic hydrocarbons |
benzene phenol chlorobenzene |
 (what is this?) (verify)Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
2-Chlorophenol or ortho-chlorophenol is an organic compound, a derivative of phenol. Related compounds are used as a disinfectant agents and various pesticides. This particular compound has few applications, but is an intermediate in the polychlorination of phenol.[5]
See also
References
Cite error: Invalid <references> tag;
parameter "group" is allowed only.
<references />, or <references group="..." />External links
- ToxFAQs for Chlorophenols, Agency for Toxic Substances and Disease Registry.
| 25px | This article about an organic halide is a stub. You can help ssf by expanding it. |
- ↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, FL: CRC Press, pp. 3–120, ISBN 0849305942
- ↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, FL: CRC Press, p. 1281, ISBN 0849305942
- ↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, FL: CRC Press, pp. 8–103, ISBN 0849305942
- ↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, FL: CRC Press, pp. 15–18, ISBN 0849305942
- ↑ Fiege, H.; Voges, H.-M.; Hamamoto, T; Umemura, S.; Iwata, T.; Miki, H.; Fujita, Y.; Buysch, H.-J.; Garbe, D.; Paulus, W. (2000), "Phenol Derivatives", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a19_313
