2,3-Xylidine: Difference between revisions
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Mefenamic acid |
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|Section1={{Chembox Identifiers |
|Section1={{Chembox Identifiers |
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| CASNo = 87-59-2 |
| CASNo = 87-59-2 |
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| EINECS = 201-755-0 |
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| PubChem = |
| PubChem = |
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| ChemSpiderID = 13840647 |
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| SMILES = |
| SMILES = Cc1cccc(c1C)N |
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| StdInChI = 1S/C8H11N/c1-6-4-3-5-8(9)7(6)2/h3-5H,9H2,1-2H3 |
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| StdInChIKey = VVAKEQGKZNKUSU-UHFFFAOYSA-N }} |
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|Section2={{Chembox Properties |
|Section2={{Chembox Properties |
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| C=8|H=11|N=1 |
| C=8|H=11|N=1 |
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Revision as of 14:40, 18 September 2017
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| Identifiers | |
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3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.001.596 |
| EC Number |
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CompTox Dashboard (EPA)
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| Properties | |
| C8H11N | |
| Molar mass | 121.183 g·mol−1 |
| Appearance | colorless liquid |
| Melting point | 3.5 °C (38.3 °F; 276.6 K) |
| Boiling point | 222 °C (432 °F; 495 K) |
| Hazards | |
| Flash point | 97 °C (207 °F; 370 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2,3-Xylidine is the organic compound with the formula C6H3(CH3)2NH2. it is one of several isomeric xylidines. It is a colorless viscous liquid. The compound is used in the production of the drug mefenamic acid and the herbicide xylachlor.[1]
References
- ^ M. Meyer (2012). "Xylidines". Ullmann's Encylclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a28_455.
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