4-Chlorobenzaldehyde
4-Chlorobenzaldehyde structure
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Common Name | 4-Chlorobenzaldehyde | ||
|---|---|---|---|---|
| CAS Number | 104-88-1 | Molecular Weight | 140.567 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 213.7±13.0 °C at 760 mmHg | |
| Molecular Formula | C7H5ClO | Melting Point | 46 °C | |
| MSDS | Chinese USA | Flash Point | 87.8±0.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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A universal quantitative ¹H nuclear magnetic resonance (qNMR) method for assessing the purity of dammarane-type ginsenosides.
Phytochem. Anal. 26(1) , 8-14, (2014) Quantitative (1)H-NMR (qNMR) is a well-established method for quantitative analysis and purity tests. Applications have been reported in many areas, such as natural products, foods and beverages, metabolites, pharmaceuticals and agriculture. The characteristi... |
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Acetalization allows the photoheterolysis of the Ar-Cl bond in chlorobenzaldehydes and chloroacetophenones.
J. Org. Chem. 77(20) , 9094-101, (2012) The nonaccessibility of phenyl cations by irradiation of electron-poor aryl chlorides was circumvented by transforming the carbonyl group of aromatic ketones or aldehydes into the corresponding 1,3-dioxolanes and the carboxyl group of benzoate ester into an o... |
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Growth of Thin, Anisotropic, π-Conjugated Molecular Films by Stepwise "Click" Assembly of Molecular Building Blocks: Characterizing Reaction Yield, Surface Coverage, and Film Thickness versus Addition Step Number.
J. Am. Chem. Soc. 137 , 8819-28, (2015) We report the systematic characterization of anisotropic, π-conjugated oligophenyleneimine (OPI) films synthesized using stepwise imine condensation, or "click" chemistry. Film synthesis began with a self-assembled monolayer (SAM) of 4-formylthiophenol or 4-a... |
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Synthesis and receptor binding assay of indolin-2-one derivatives as dopamine D4 receptor ligands.
Pharmazie 70 , 511-4, (2015) Five indolin-2-one derivatives bearing piperazinylbutyl side chains attached to the amide nitrogen were synthesized from 2-indolinone. 1-(4-Bromobutyl)-indolin-2-one was reacted with 1-piperazinecarboxaldehyde to form 1-(4-(4-formyl-1-piperazinyl)butyl)indoli... |
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Experimental and theoretical studies of the products of addition-elimination reactions between benzil dihydrazone and three isomeric chlorobenzaldehydes.
Acta Crystallogr. C Struct. Chem. 71 , 554-63, (2015) A series of mono- and di-Schiff bases formed between benzil dihydrazone {BDH; systematic name: (1Z)-[(2E)-2-hydrazinylidene-1,2-diphenylethylidene]hydrazine} and three isomeric chlorobenzaldehydes were designed and synthesized to be used as model compounds to... |
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(E)-3-tert-butyl-4-(4-chlorobenzyl)-N-(4-chlorobenzylidene)-1-phenyl-1H-pyrazol-5-amine: sheets built from π-stacked hydrogen-bonded dimers.
Acta Crystallogr. C 69(Pt 9) , 1039-42, (2013) The title compound, C27H25Cl2N3, is an unexpected but high-yield product from the microwave-mediated reaction between 3-tert-butyl-N-4-chlorobenzyl-1-phenyl-1H-pyrazol-5-amine and 4-chlorobenzaldehyde. Inversion-related pairs of molecules are linked by C-H···... |
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First Novozym 435 lipase-catalyzed Morita-Baylis-Hillman reaction in the presence of amides.
Enzyme Microb. Technol. 84 , 32-40, (2016) The first Novozym 435 lipase-catalyzed Morita-Baylis-Hillman (MBH) reaction with amides as co-catalyst was realized. Results showed that neither Novozym 435 nor amide can independently catalyze the reaction. This co-catalytic system that used a catalytic amou... |
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[Experimental substantiation of an approximate safe level of p-chlorobenzaldehyde in the air of the work area].
Gig. Tr. Prof. Zabol. (2) , 50-1, (1987)
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An efficient, multicomponent approach for solvent-free synthesis of 2-amino-4H-chromene scaffold.
Mol. Divers. 14(3) , 473-7, (2010) Solvent-free one-pot synthesis of 2-amino-4H-chromene scaffold is described in a very simple, efficient, and environmentally benign method using sodium carbonate as a cheap and non-toxic catalyst with up to excellent yields. |
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Toward the development of chemoprevention agents. Part 1: Design, synthesis, and anti-inflammatory activities of a new class of 2,5-disubstituted-dioxacycloalkanes.
Bioorg. Med. Chem. 15 , 4775-99, (2007) A new class of 2,5-disubstituted-dioxacycloalkanes were designed and synthesized via stereoselective synthetic method as cancer chemoprevention agents. The anti-inflammatory activities of these compounds were tested using the xylene-induced mouse ear edema mo... |