- 2-Iodobenzaldehyde
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- $0.00 / 1g
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2026-02-02
- CAS:26260-02-6
- Min. Order: 10mg
- Purity: 99%HPLC
- Supply Ability: 2000tons
- 2-Iodobenzaldehyde
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- $0.00 / 1KG
-
2025-04-04
- CAS:26260-02-6
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 1Ton
- 2-IODOBENZALDEHYDE
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- $6.60 / 1KG
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2020-01-03
- CAS:26260-02-6
- Min. Order: 1KG
- Purity: 97%-99%
- Supply Ability: 1kg -1000kg
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| | 2-IODOBENZALDEHYDE Basic information |
| | 2-IODOBENZALDEHYDE Chemical Properties |
| Melting point | 36-39 °C (lit.) | | Boiling point | 129 °C (14 mmHg) | | density | 1.8576 (estimate) | | Fp | >230 °F | | storage temp. | 2-8°C | | solubility | soluble in Methanol | | form | Low Melting Crystalline Mass or Powder | | color | White to light beige | | Sensitive | Light Sensitive | | BRN | 1927296 | | InChI | InChI=1S/C7H5IO/c8-7-4-2-1-3-6(7)5-9/h1-5H | | InChIKey | WWKKTHALZAYYAI-UHFFFAOYSA-N | | SMILES | C(=O)C1=CC=CC=C1I | | CAS DataBase Reference | 26260-02-6(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | HazardClass | IRRITANT, AIR SENSITIVE, KEEP COLD | | HS Code | 29130000 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 2-IODOBENZALDEHYDE Usage And Synthesis |
| Chemical Properties | white to light beige low melting crystalline | | Uses | 2-Iodo-benzaldehyde is a very useful synthetic intermediate. It is halogenated Benzaldehyde (B119740) which is mainly used as a precursor to other organic compounds, such as pharmaceuticals, and plastic additives. | | Uses | 2-Iodobenzaldehyde may be used as a reactant in the synthesis of the following heterocycles:
- 2,3-diaryl-1-indenones
- indolo[1,2-a]quinazolines
- Baylis-Hillman (BH) adducts
It may also be used in preparing:
- 5-phenylindazolo[3,2-b]quinazolin-7(5H)-one
- 4-(3-iodophenyl)-2,2:6,2-terpyridine
- fluoren-9-one
- 2-formyl-3′-methoxybiphenyl
| | General Description | 2-Iodobenzaldehyde (o-iodobenzaldehyde) is a 2-halobenzaldehyde derivative. Its crystals belong to the orthorhombic crystal system and P212121 space group. | | Synthesis | General procedure for the synthesis of 2-iodobenzaldehyde from 2-formylphenylboronic acid: 2-formylphenylboronic acid (0.067 g, 0.4 mmol), copper powder (0.0052 g, 0.08 mmol), (CF3)2CFI (0.178 g, 0.6 mmol) and DMF (2 mL) were added to a closed tube with a rubber stopper. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the resulting suspension was poured into water and extracted with ethyl acetate. The organic layers were combined, dried with anhydrous Na2SO4 and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography using petroleum ether/ethyl acetate (20:1, v/v) as eluent to give 0.086 g of 2-iodobenzaldehyde as a light yellow solid (0.35 mmol, 87% yield). | | References | [1] Journal of Fluorine Chemistry, 2016, vol. 189, p. 59 - 67 |
| | 2-IODOBENZALDEHYDE Preparation Products And Raw materials |
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