- 2-Allylphenol
-
- $8.00
-
2026-09-02
- CAS:1745-81-9
- Min. Order: 1KG
- Purity: 99%
- 2-Allylphenol
-
- $57.00
-
2026-08-08
- CAS:1745-81-9
- Purity: 99.74%
- Supply Ability: 10g
- 2-Allylphenol
-
-
2026-06-30
- CAS:1745-81-9
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1000kg
|
| | 2-Allylphenol Basic information |
| | 2-Allylphenol Chemical Properties |
| Melting point | -6 °C | | Boiling point | 220 °C (lit.) | | density | 1.028 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.546(lit.) | | Fp | 192 °F | | storage temp. | Inert atmosphere,Room Temperature | | solubility | 7 g/L (20°C) | | pka | pK1: 10.28 (25°C) | | form | Oil | | color | Colourless | | PH | 6-7 (100g/l, H2O, 20℃) | | Water Solubility | 7 g/L (20 ºC) | | BRN | 742121 | | InChI | 1S/C9H10O/c1-2-5-8-6-3-4-7-9(8)10/h2-4,6-7,10H,1,5H2 | | InChIKey | QIRNGVVZBINFMX-UHFFFAOYSA-N | | SMILES | Oc1ccccc1CC=C | | LogP | 2.91 | | Dissociation constant | 10.27-10.29 at 25℃ | | CAS DataBase Reference | 1745-81-9(CAS DataBase Reference) | | NIST Chemistry Reference | Phenol, 2-(2-propenyl)-(1745-81-9) | | EPA Substance Registry System | Phenol, 2-(2-propenyl)- (1745-81-9) |
| Hazard Codes | C,Xi | | Risk Statements | 21/22-34-36/38 | | Safety Statements | 26-36/37/39-45-24/25-23 | | RIDADR | UN 2923 8/PG 3 | | WGK Germany | 2 | | RTECS | SJ3850000 | | TSCA | TSCA listed | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29071900 | | Storage Class | 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials | | Hazard Classifications | Acute Tox. 3 Dermal
Acute Tox. 3 Oral
Eye Dam. 1
Skin Corr. 1B |
| | 2-Allylphenol Usage And Synthesis |
| Description | 2-ally phenol is a fungicide. Little information is available regarding its environmental fate nor its toxicity to biodiversity. No information has been found on its toxicity to humans. | | Chemical Properties | clear colourless to light yellow liquid | | Uses | 2-Allylphenol is an protected intermediate in the synthesis of metabolites of Diclofenac (D436450), a nonsteroidal anti-inflammatory compound an decycloxygenase (COX) inhibitor. | | Production Methods | Commercial production of 2 allylphenol is essentially the manufacture of a simple substituted phenol rather than a multi step pesticide synthesis. Industrial routes typically begin with ortho cresol or phenol derivatives, which undergo Friedel–Crafts type alkylation or transition metal catalysed allylation to introduce the allyl side chain at the ortho position. Catalysts such as Lewis acids or palladium complexes are used to control regioselectivity and suppress rearrangement to propenylphenols. The crude product is then purified by fractional distillation to remove unreacted phenol | | Definition | ChEBI: A member of the class of phenols that is phenol carrying an allyl group at position 2. | | Synthesis Reference(s) | Synthesis, p. 310, 1981 DOI: 10.1055/s-1981-29431
Tetrahedron Letters, 35, p. 1409, 1994 DOI: 10.1016/S0040-4039(00)76231-9 | | Mechanism of action | Inhibits the fungal pathogen by inhibiting respriation | | Pesticide Type | Fungicide |
| | 2-Allylphenol Preparation Products And Raw materials |
|