The Bromoform with CAS registry number of 75-25-2 is also known as Methane, tribromo-. The IUPAC name and product name are the same. It belongs to product categories of Pharmaceutical Intermediates; Organics; Heterocyclic Compounds; Analytical Chemistry; Solvents for HPLC & Spectrophotometry; Solvents for Spectrophotometry; Standard Solution of Volatile Organic Compounds for Water & Soil Analysis; Standard Solutions (VOC); 600 Series Wastewater Methods; A-BAlphabetic; Alpha Sort; B; BI - BZChemical Class; BromoEPA; Halogenated; Method 601; Volatiles/ Semivolatiles. Its EINECS registry number is 200-854-6. In addition, the formula is CHBr₃ and the molecular weight is 252.73.

Physical properties about Bromoform are: (1)ACD/LogP: 2.29; (2)ACD/LogD (pH 5.5): 2.29; (3)ACD/LogD (pH 7.4): 2.29; (4)ACD/BCF (pH 5.5): 32.39; (5)ACD/BCF (pH 7.4): 32.39; (6)ACD/KOC (pH 5.5): 419.56; (7)ACD/KOC (pH 7.4): 419.56; (8)Index of Refraction: 1.619; (9)Molar Refractivity: 29.83 cm³; (10)Molar Volume: 84.9 cm³; (11)Surface Tension: 49.8 dyne/cm; (12)Density: 2.974 g/cm³; (13)Flash Point: 44 °C; (14)Enthalpy of Vaporization: 39.66 kJ/mol; (15)Boiling Point: 149.2 °C at 760 mmHg; (16)Vapour Pressure: 5.17 mmHg at 25 °C.

Preparation of Bromoform: it is prepared by reaction of acetone with sodium hypobromite under alkaline conditions. Then product is derived after decomposition, distillation, washing, filtration and drying.

Uses of Bromoform: it is used to produce 1,1-dibromo-2-phenyl-cyclopropane by reaction with vinylbenzene. The reaction occurs with reagent potassium tert-butoxide and solvent pentane at ambient temperature for 10 hours. The yield is about 65%. This cehmical is also can be used as dye intermediate, disinfectant, analgesic, anesthetic, refrigerant, mineral agent, precipitating agent, solvent and liquid component of  blast-resistant.

When you are using this chemical, please be cautious about it. As a chemical, it is irritating to eyes and skin. It's toxic to aquatic organisms and may cause long-term adverse effects in the aquatic environment. What's more, it has danger of very serious irreversible effects through inhalation, in contact with skin and if swallowed. During using it, wear suitable protective clothing and gloves. Avoid release to the environment. In case of accident or if you feel unwell seek medical advice immediately. After using it, keep container tightly closed  and away from sources of ignition. After contact with skin, wash immediately.

You can still convert the following datas into molecular structure:
1. Canonical SMILES: C(Br)(Br)Br
2. InChI: InChI=1S/CHBr3/c2-1(3)4/h1H
3. InChIKey: DIKBFYAXUHHXCS-UHFFFAOYSA-N

The toxicity data is as follows: