4-Chlorobenzaldehyde

4-Chlorobenzaldehyde
Identifiers
CAS Number	104-88-1 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL1474;
ECHA InfoCard	100.002.953
EC Number	203-247-4;
KEGG	C06648;
PubChem CID	7726;
UNII	E67727UP9Z;
UN number	2811
CompTox Dashboard (EPA)	DTXSID2021860 ;
	InChI InChI=1S/C7H5ClO/c8-7-3-1-6(5-9)2-4-7/h1-5H Key: AVPYQKSLYISFPO-UHFFFAOYSA-N;
	SMILES C1=CC(=CC=C1C=O)Cl;
Properties
Chemical formula	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
	GHS labelling:[1]
Pictograms
Signal word	Warning
Hazard statements	H302, H315, H317, H319, H411
Precautionary statements	P261, P264, P264+P265, P270, P271, P272, P273, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P333+P313, P337+P317, P362+P364, P391, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

4-Chlorobenzaldehyde is an organic compound with the chemical formula C₇H₅ClO. It can 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". pubchem.ncbi.nlm.nih.gov. Retrieved 3 April 2022.
Y. X. Yang, X. Q. An, M. Kang, W. Zeng, Z. W. Yang, H. C. Ma (March 2020). "A Simple and Effective Method for Catalytic Oxidation of Alcohols Using the Oxone/Bu4NHSO4 Oxidation System". Russian Journal of Organic Chemistry. 56 (3): 521–523. doi:10.1134/S1070428020030240. ISSN 1070-4280. S2CID 216049138. Retrieved 2021-05-10.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Juan V. Alegre-Requena, Eugenia Marqués-López, Raquel P. Herrera (2018-01-04). "Organocatalyzed Enantioselective Aldol and Henry Reactions Starting from Benzylic Alcohols". Advanced Synthesis & Catalysis. 360 (1): 124–129. doi:10.1002/adsc.201701351. S2CID 102499775. Retrieved 2021-05-10.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Mahdi Hajimohammadi, Naeleh Azizi, Sajjad Tollabimazraeno, Ali Tuna, Jiri Duchoslav, Günther Knör (January 2021). "Cobalt (II) Phthalocyanine Sulfonate Supported on Reduced Graphene Oxide (RGO) as a Recyclable Photocatalyst for the Oxidation of Aldehydes to Carboxylic Acids". Catalysis Letters. 151 (1): 36–44. doi:10.1007/s10562-020-03287-9. ISSN 1011-372X. S2CID 220312197. Retrieved 2021-05-10.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Ziyang Gao, Hongyuan Yang, Qing Liu (October 2019). "Natural Seashell Waste as an Efficient and Low‐Cost Catalyst for the Synthesis of Arylmethylenemalonitriles". CLEAN – Soil, Air, Water. 47 (10): 1900129. doi:10.1002/clen.201900129. ISSN 1863-0650. S2CID 203946880. Retrieved 2021-05-10.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Meixia He, Jean-Marie Lehn (2019-11-20). "Time-Dependent Switching of Constitutional Dynamic Libraries and Networks from Kinetic to Thermodynamic Distributions". Journal of the American Chemical Society. 141 (46): 18560–18569. doi:10.1021/jacs.9b09395. ISSN 0002-7863. PMID 31714075. S2CID 207938797. Retrieved 2021-05-10.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] "4-Chlorobenzaldehyde". pubchem.ncbi.nlm.nih.gov. Retrieved 3 April 2022.

[2] Y. X. Yang, X. Q. An, M. Kang, W. Zeng, Z. W. Yang, H. C. Ma (March 2020). "A Simple and Effective Method for Catalytic Oxidation of Alcohols Using the Oxone/Bu4NHSO4 Oxidation System". Russian Journal of Organic Chemistry. 56 (3): 521–523. doi:10.1134/S1070428020030240. ISSN 1070-4280. S2CID 216049138. Retrieved 2021-05-10.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[3] Juan V. Alegre-Requena, Eugenia Marqués-López, Raquel P. Herrera (2018-01-04). "Organocatalyzed Enantioselective Aldol and Henry Reactions Starting from Benzylic Alcohols". Advanced Synthesis & Catalysis. 360 (1): 124–129. doi:10.1002/adsc.201701351. S2CID 102499775. Retrieved 2021-05-10.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[4] Mahdi Hajimohammadi, Naeleh Azizi, Sajjad Tollabimazraeno, Ali Tuna, Jiri Duchoslav, Günther Knör (January 2021). "Cobalt (II) Phthalocyanine Sulfonate Supported on Reduced Graphene Oxide (RGO) as a Recyclable Photocatalyst for the Oxidation of Aldehydes to Carboxylic Acids". Catalysis Letters. 151 (1): 36–44. doi:10.1007/s10562-020-03287-9. ISSN 1011-372X. S2CID 220312197. Retrieved 2021-05-10.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[5] Ziyang Gao, Hongyuan Yang, Qing Liu (October 2019). "Natural Seashell Waste as an Efficient and Low‐Cost Catalyst for the Synthesis of Arylmethylenemalonitriles". CLEAN – Soil, Air, Water. 47 (10): 1900129. doi:10.1002/clen.201900129. ISSN 1863-0650. S2CID 203946880. Retrieved 2021-05-10.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[6] Meixia He, Jean-Marie Lehn (2019-11-20). "Time-Dependent Switching of Constitutional Dynamic Libraries and Networks from Kinetic to Thermodynamic Distributions". Journal of the American Chemical Society. 141 (46): 18560–18569. doi:10.1021/jacs.9b09395. ISSN 0002-7863. PMID 31714075. S2CID 207938797. Retrieved 2021-05-10.