4,5-DIBROMO-1-TRIPHENYLMETHYL-1H-IMIDAZOLE

The 1H-Imidazole,4,5-dibromo-1-(triphenylmethyl)-, with the CAS registry number 112517-23-4, is also known as 4,5-Dibromo-1-triphenylmethyl-1H-imidazole. It belongs to the product categories of Blocks; Bromides; Imidazoles. This chemical's molecular formula is C₂₂H₁₆Br₂N₂ and molecular weight is 468.18. What's more, its systematic name is called 4,5-Dibromo-1-trityl-imidazole. When you are dealing with this chemical, you should be very careful. This chemical may cause inflammation to the skin or other mucous membranes.

Physical properties about 1H-Imidazole,4,5-dibromo-1-(triphenylmethyl)- are: (1)ACD/LogP: 6.30; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): 6.3; (4)ACD/LogD (pH 7.4): 6.3; (5)#H bond acceptors: 2; (6)#H bond donors: 0; (7)#Freely Rotating Bonds: 4; (8)Polar Surface Area: 17.82 Å²; (9)Index of Refraction: 1.651; (10)Molar Refractivity: 116.39 cm³; (11)Molar Volume: 318.5 cm³; (12)Surface Tension: 48.4 dyne/cm; (13)Density: 1.46 g/cm³; (14)Flash Point: 276.4 °C; (15)Enthalpy of Vaporization: 77.9 kJ/mol; (16)Boiling Point: 533.4 °C at 760 mmHg; (17)Vapour Pressure: 6.4E-11 mmHg at 25 °C.

Preparation of 1H-Imidazole,4,5-dibromo-1-(triphenylmethyl)-: this chemical can be prepared by 4,5-Dibromo-1H-imidazole with Chloro-triphenyl-methane. This reaction needs reagent Triethylamine and solvent Benzene. The yield is 91 %.

Uses of 1H-Imidazole,4,5-dibromo-1-(triphenylmethyl)-: it is used to produce other chemicals. For example, it is used to produce 4,5-Dibromo-1H-imidazole. The reaction occurs with reagent Acetic acid, solvent Methanol and other condition of heating for 4 hours. The yield is 77 %.

You can still convert the following datas into molecular structure:
(1) SMILES: c1ccc(cc1)C(c2ccccc2)(c3ccccc3)n4cnc(c4Br)Br
(2) InChI: InChI=1/C22H16Br2N2/c23-20-21(24)26(16-25-20)22(17-10-4-1-5-11-17,18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-16H
(3) InChIKey: ZHVSCWZZBQRLCU-UHFFFAOYAR