Identification | More | [Name]
3-Iodobenzaldehyde | [CAS]
696-41-3 | [Synonyms]
3-IODOBENZALDEHYDE 3-IODOBENZALDEHYDE, 99+% | [EINECS(EC#)]
626-706-4 | [Molecular Formula]
C7H5IO | [MDL Number]
MFCD00039573 | [Molecular Weight]
232.02 | [MOL File]
696-41-3.mol |
Chemical Properties | Back Directory | [Appearance]
Pale yellow crystalline powder | [Melting point ]
57-60 °C (lit.) | [Boiling point ]
124-125°C 13mm | [density ]
1.8576 (estimate) | [Fp ]
124-125°C/13mm | [storage temp. ]
Keep Cold | [form ]
Crystalline Powder, Crystals or Needles | [color ]
White to pale yellow | [Water Solubility ]
Slightly soluble in water. | [Sensitive ]
Air & Light Sensitive | [BRN ]
1854653 | [InChIKey]
RZODAQZAFOBFLS-UHFFFAOYSA-N | [CAS DataBase Reference]
696-41-3(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT, AIR SENSITIVE, KEEP COLD | [HS Code ]
29130000 |
Hazard Information | Back Directory | [Chemical Properties]
Pale yellow crystalline powder | [Uses]
3-Iodobenzaldehyde is used as an organic reagent. | [General Description]
3-Iodobenzaldehyde can be prepared by the iodination of benzaldehyde using 1,3-diiodo-5,5-dimethylhydantoin in sulfuric acid. | [Synthesis]
3-Iodobenzaldehyde (12) was synthesized as follows: pyridinium chlorochromate (2.45 g, 11.4 mmol) and dry diatomaceous earth (about 2.00 g) were suspended in anhydrous dichloromethane (20 ml) at room temperature and stirred for 15 minutes. Subsequently, a solution of 3-iodobenzyl alcohol (11) (1.02 g, 4.35 mmol) in anhydrous dichloromethane (5 ml) was added to this suspension. The reaction mixture was protected from light and stirring was continued for 2 hours at room temperature. After completion of the reaction, the reaction solution was diluted with ether and filtered through diatomaceous earth. The resulting turbid brown filtrate was concentrated to a reddish brown gelatinous paste, which was redissolved in dichloromethane and purified by short silica gel column chromatography using dichloromethane as eluent. A clarified colorless solution was finally obtained, and 3-iodobenzaldehyde (12) was concentrated to give 3-iodobenzaldehyde (12) as a white solid (0.953 g, 95% yield).1H NMR (400 MHz, CDCl3) data were as follows: δ 7.29 (t, J = 7.8 Hz, 1H, H5); 7.85 (br d, J = 7.8 Hz, 1H, H6); 7.96 (br d, J =7.8 Hz, 1H, H4); 8.21 (br s, 1H, H2); 9.93 (s, 1H, CHO). | [References]
[1] Advanced Synthesis and Catalysis, 2004, vol. 346, # 7, p. 767 - 776 [2] Patent: WO2005/82894, 2005, A1. Location in patent: Page/Page column 41-42 [3] Bulletin of the Chemical Society of Ethiopia, 2013, vol. 27, # 1, p. 131 - 136 [4] Bioorganic and Medicinal Chemistry Letters, 1999, vol. 9, # 20, p. 3047 - 3052 [5] Tetrahedron Asymmetry, 2001, vol. 12, # 4, p. 585 - 596 |
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