Revision as of 20:05, 19 January 2025 editSmokefoot (talk | contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers75,107 edits updated (still quite old) prep← Previous edit | Latest revision as of 08:07, 20 January 2025 edit undoGraeme Bartlett (talk | contribs)Administrators250,307 edits more ids and hazards from pubchem | ||
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|Section1={{Chembox Identifiers | |Section1={{Chembox Identifiers | ||
| CASNo = 1849-36-1 | | CASNo = 1849-36-1 | ||
| CASNo_Ref = {{Cascite|correct|CAS}} | |||
| CASNo_Comment = | |||
| |
| ChEMBL = 120606 | ||
| |
| ChemSpiderID = 15030 | ||
| EC_number = 217-436-4 | |||
| PubChem = 15809 | | PubChem = 15809 | ||
| |
| UNII = QL9H28763R | ||
| StdInChI=1S/C6H5NO2S/c8-7(9)5-1-3-6(10)4-2-5/h1-4,10H | |||
| StdInChIKey = AXBVSRMHOPMXBA-UHFFFAOYSA-N | |||
| SMILES = C1=CC(=CC=C1(=O))S | |||
}} | |||
|Section2={{Chembox Properties | |Section2={{Chembox Properties | ||
| C=6|H=5|S=1|N=1|O=2 | | C=6|H=5|S=1|N=1|O=2 | ||
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| Solubility = alcohols}} | | Solubility = alcohols}} | ||
|Section3={{Chembox Hazards | |Section3={{Chembox Hazards | ||
| GHS_ref= | |||
| GHSPictograms = {{GHS07}} | |||
| GHSSignalWord = Warning | |||
| HPhrases = {{H-phrases|315|319|335}} | |||
| PPhrases = {{P-phrases|261|264|264+265|271|280|302+352|304+340|305+351+338|319|321|332+317|337+317|362+364|403+233|405|501}} | |||
| MainHazards = | | MainHazards = | ||
| FlashPt = | | FlashPt = |
Latest revision as of 08:07, 20 January 2025
Names | |
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Other names 4-nitrobenzenethiol | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.015.852 |
EC Number |
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PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C6H5NO2S |
Molar mass | 155.17 g·mol |
Appearance | yellow solid |
Density | 1.362 g/cm |
Melting point | 79–80 °C (174–176 °F; 352–353 K) |
Solubility in water | alcohols |
Hazards | |
GHS labelling: | |
Pictograms | |
Signal word | Warning |
Hazard statements | H315, H319, H335 |
Precautionary statements | P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
4-Nitrothiophenol is an organosulfur compound with the formula HSC6H4NO2. It exists as a yellow solid that is soluble in several organic solvents. It is one of three isomers of nitrothiophenol. It was originally prepared by sulfidation of 4-nitrochlorobenzene, which was improved by intentionally generating a polysulfide intermediate. 4-Nitrothiophenol is closely related to thiophenol but more acidic.
The compound reacts with chlorine to give 4-nitrophenylsulfenyl chloride, a useful reagent. It has also been used as a probe of plasmon-induced reactions.
References
- Fromm, E.; Wittmann, J. (1908). "Derivate des p -Nitrothiophenols I. Einwirking von Schwefel und Alkali auf p-Nitrochlorobenzol". Berichte der Deutschen Chemischen Gesellschaft. 41 (2): 2264–2273. doi:10.1002/cber.190804102131.
- Price, Charles C.; Stacy, Gardner W. (1946). "P-Nitrophenyl Disulfide, p-Nitrophenyl Sulfide and p-Nitrothiophenol". Journal of the American Chemical Society. 68 (3): 498–500. Bibcode:1946JAChS..68..498P. doi:10.1021/ja01207a042.
- Kim, Sunggak (2007). "4-Nitrobenzenesulfenyl Chloride". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/9780470842898.rn00720. ISBN 978-0-471-93623-7.
- Sun, Mengtao; Xu, Hongxing (2012). "A Novel Application of Plasmonics: Plasmon-Driven Surface-Catalyzed Reactions". Small. 8 (18): 2777–2786. doi:10.1002/smll.201200572. PMID 22777813.