Reported in EPA TSCA Inventory.
The 2-Isopropyl-4-methylphenol is an organic compound with the formula C10H14O. The IUPAC name of this chemical is 4-methyl-2-propan-2-ylphenol. With the CAS registry number 4427-56-9, it is also named as Phenol, 4-methyl-2-(1-methylethyl)-. The classification codes are Mutation data and Tumor data. When heated to decomposition it emits acrid smoke and fumes.
The other characteristics of this product can be summarized as: (1)ACD/LogP: 3.28; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.28; (4)ACD/LogD (pH 7.4): 3.28; (5)ACD/BCF (pH 5.5): 183.42; (6)ACD/BCF (pH 7.4): 183.35; (7)ACD/KOC (pH 5.5): 1451.39; (8)ACD/KOC (pH 7.4): 1450.8; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 2; (12)Index of Refraction: 1.523; (13)Molar Refractivity: 47.14 cm3; (14)Molar Volume: 154.2 cm3; (15)Polarizability: 18.68×10-24 cm3; (16)Surface Tension: 34.9 dyne/cm; (17)Enthalpy of Vaporization: 48.4 kJ/mol; (18)Vapour Pressure: 0.0486 mmHg at 25°C; (19)Rotatable Bond Count: 1; (20)Tautomer Count: 3; (21)Exact Mass: 150.104465; (22)MonoIsotopic Mass: 150.104465; (23)Topological Polar Surface Area: 20.2; (24)Heavy Atom Count: 11; (25)Complexity: 120.
Preparation of 2-Isopropyl-4-methylphenol: It can be obtained by 4-hydroxy-3-(1-methylethyl)benzaldehyde. This reaction needs reagent N2H4*H2O, KOH and solvent bis-(2-hydroxy-ethyl) ether at temperature of 210 °C. The reaction time is 1 hours. The yield is 82%.
Uses of 2-Isopropyl-4-methylphenol: It can react with propionic acid anhydride to get 4-methyl-2-(1-methylethyl)phenyl propanoate. The yield is 96%
People can use the following data to convert to the molecule structure.
1. SMILES:Oc1ccc(cc1C(C)C)C
2. InChI:InChI=1/C10H14O/c1-7(2)9-6-8(3)4-5-10(9)11/h4-7,11H,1-3H3
3. InChIKey:DSTPUJAJSXTJHM-UHFFFAOYAY
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