| Weight | 175.014 g/mol |
|---|---|
| Formula | C7H4Cl2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,3-Dichlorobenzaldehyde (6334-18-5, 31155-09-6)
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- Polymeric pesticides, 3. Synthesis and characterization of polyacetals prepared from ,diols and 2,6dichlorobenzaldehyde (Macromolecular Chemistry and Physics, 1978)
- Calculated on 1H and 13C NMR chemical shifts of 2,4difluorobenzaldehyde isonicotinoylhydrazone and 2,3dichlorobenzaldehyde isonicotinoylhydrazone with GIAO, IGAIM, and CSGT models (Concepts in Magnetic Resonance Part A, 2009)
- Synthesis of some diamides of 2-chlorobenzaldehyde, 2,4-dichlorobenzaldehyde, and 3,4-dichlorobenzaldehyde (Journal of Pharmaceutical Sciences, 1965)
- Photochromic heterocyclic fulgides. Part 8. The condensation of 2,6-dichlorobenzaldehyde with diethyl [1-(2,5-dimethyl-3-furyl)ethylidene]succinate to give 6-chloro-2-(2,5-dimethyl-3-furyl)-1H-benzocycloheptene-3,4-dicarboxylic anhydride and photochromic (7S,7aS)-7-(2,6-dichlorophenyl)-2,4,7a-trimethyl-7,7a-dihydrobenzofuran-5,6-dicarboxylic anhydride (Journal of The Chemical Society-perkin Transactions 1, 1995)
- NMR Chemical Shifts of 2,4-Difluorobenzaldehyde Isonicotinoylhydrazone and 2,3-Dichlorobenzaldehyde Isonicotinoylhydrazone with GIAO, IGAIM, and CSGT Models (2009)
- ChemInform Abstract: Photochromic Heterocyclic Fulgides. Part 8. Condensation of 2,6 Dichlorobenzaldehyde with Diethyl (1(2,5Dimethyl3furyl)ethylidene) succinate to Give 6Chloro2(2,5dimethyl3furyl)1H benzocycloheptene3,4dicarboxylic Anhydride and Photochromic (7S,7aS) 7(2,6Dichlorophenyl)2,4,7atrimethyl7,7adihydrobenzofuran5,6 dicarboxylic Anhydride. (ChemInform, 2010)
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SMILESC1=CC(=C(C(=C1)Cl)Cl)C=O
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InChIKeyLLMLNAVBOAMOEE-UHFFFAOYSA-N
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