Chemistry:4-Chlorobenzaldehyde
From HandWiki
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| UNII | |
| UN number | 2811 |
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| Properties | |
| C7H5ClO | |
| Molar mass | 140.57 g·mol−1 |
| Melting point | 47.5 °C (117.5 °F; 320.6 K) |
| Boiling point | 213.5 °C (416.3 °F; 486.6 K) |
| Hazards | |
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| GHS Signal word | Warning |
| H302, H315, H317, H319, H411 | |
| P261, P264, P264+265Script error: No such module "Preview warning".Category:GHS errors, P270, P271, P272, P273, P280, P301+317Script error: No such module "Preview warning".Category:GHS errors, P302+352, P304+340, P305+351+338, P319Script error: No such module "Preview warning".Category:GHS errors, P321, P330, P332+317Script error: No such module "Preview warning".Category:GHS errors, P333+313, P337+317Script error: No such module "Preview warning".Category:GHS errors, P362+364Script error: No such module "Preview warning".Category:GHS errors, P391, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Tracking categories (test):
4-Chlorobenzaldehyde is an organic compound with the chemical formula C7H5ClO. It can be produced by the oxidation of 4-chlorobenzyl alcohol.[2][3] It can be further oxidized to 4-chlorobenzoic acid.[4] It will react with malononitrile to form 4-chlorobenzylidenylmalononitrile. [5]4-Chlorobenzaldehyde reacts with benzylamine to produce N-(4-chlorobenzylidenyl)benzylamine。[6]
References
- ↑ "4-Chlorobenzaldehyde" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/7726#section=Safety-and-Hazards.
- ↑ Yang, Y. X.; An, X. Q.; Kang, M.; Zeng, W.; Yang, Z. W.; Ma, H. C. (2020). "A Simple and Effective Method for Catalytic Oxidation of Alcohols Using the Oxone/Bu4NHSO4 Oxidation System" (in en). Russian Journal of Organic Chemistry 56 (3): 521–523. doi:10.1134/S1070428020030240. ISSN 1070-4280. https://link.springer.com/10.1134/S1070428020030240. Retrieved 2021-05-10.
- ↑ Alegre-Requena, Juan V.; Marqués-López, Eugenia; Herrera, Raquel P. (2018-01-04). "Organocatalyzed Enantioselective Aldol and Henry Reactions Starting from Benzylic Alcohols" (in en). Advanced Synthesis & Catalysis 360 (1): 124–129. doi:10.1002/adsc.201701351. ISSN 1615-4150. https://onlinelibrary.wiley.com/doi/10.1002/adsc.201701351. Retrieved 2021-05-10.
- ↑ Hajimohammadi, Mahdi; Azizi, Naeleh; Tollabimazraeno, Sajjad; Tuna, Ali; Duchoslav, Jiri; Knör, Günther (2021). "Cobalt (II) Phthalocyanine Sulfonate Supported on Reduced Graphene Oxide (RGO) as a Recyclable Photocatalyst for the Oxidation of Aldehydes to Carboxylic Acids" (in en). Catalysis Letters 151 (1): 36–44. doi:10.1007/s10562-020-03287-9. ISSN 1011-372X. https://link.springer.com/10.1007/s10562-020-03287-9. Retrieved 2021-05-10.
- ↑ Gao, Ziyang; Yang, Hongyuan; Liu, Qing (2019). "Natural Seashell Waste as an Efficient and Low-Cost Catalyst for the Synthesis of Arylmethylenemalonitriles" (in en). CLEAN – Soil, Air, Water 47 (10): 1900129. doi:10.1002/clen.201900129. ISSN 1863-0650. https://onlinelibrary.wiley.com/doi/10.1002/clen.201900129. Retrieved 2021-05-10.
- ↑ He, Meixia; Lehn, Jean-Marie (2019-11-20). "Time-Dependent Switching of Constitutional Dynamic Libraries and Networks from Kinetic to Thermodynamic Distributions" (in en). Journal of the American Chemical Society 141 (46): 18560–18569. doi:10.1021/jacs.9b09395. ISSN 0002-7863. PMID 31714075. https://pubs.acs.org/doi/10.1021/jacs.9b09395. Retrieved 2021-05-10.
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