Identification | Back Directory | [Name]
5-BROMO-1H-BENZOTRIAZOLE | [CAS]
32046-62-1 | [Synonyms]
5-BROMOBENZOTRIAZOLE 5-BROMO-1H-BENZOTRIAZOLE 6-Bromo-1H-benzotriazole 5-bromo-2H-benzotriazole 5-Bromo-1H-benzotraizole 1H-Benzotriazole, 5-bromo- 1H-Benzotriazole, 6-broMo- 5-Bromo-1H-1,2,3-benzotriazole 6-Bromo-1H-1,2,3-benzotriazole 1H-1,2,3-benzotriazole, 5-bromo- 5-Bromo-1H-benzo[d][1,2,3]triazole 5-bromo-1H-1,2,3-benzotriazole(SALTDATA: FREE) 5-BROMO BENZOTRIAZOLE , (5-Bromo-1H-Benzotriazole) | [Molecular Formula]
C6H4BrN3 | [MDL Number]
MFCD00464510 | [MOL File]
32046-62-1.mol | [Molecular Weight]
198.02 |
Chemical Properties | Back Directory | [Boiling point ]
416.6±18.0 °C(Predicted) | [density ]
1.894±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
solid | [pka]
7.45±0.40(Predicted) | [color ]
White to yellow | [InChI]
InChI=1S/C6H4BrN3/c7-4-1-2-5-6(3-4)9-10-8-5/h1-3H,(H,8,9,10) | [InChIKey]
BQCIJWPKDPZNHD-UHFFFAOYSA-N | [SMILES]
N1C2=CC(Br)=CC=C2N=N1 |
Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 5-bromo-1H-benzotriazole from 4-bromo-o-phenylenediamine was as follows: 4-bromobenzene-1,2-diamine (10 g, 53.5 mmol) was dissolved in a mixture of acetic acid (20 ml, 349 mmol) and water (100 ml) in an ice-bath at 0-5 °C. A solution of sodium nitrite (4.06 g, 58.8 mmol) in water (10 ml) was added slowly and dropwise. The ice bath condition was maintained and the reaction mixture was stirred for 1 hour. Subsequently, additional acetic acid (20 ml, 349 mmol) was added and the reaction system was heated to 80-85°C and stirring was continued for 1 hour. Upon completion of the reaction, the hot solution was filtered to remove insoluble black impurities. The filtrate was cooled to 0-5 °C and left to age for 30 min. The precipitate precipitated was washed with water and dried under vacuum at 45 °C to afford the target product 5-bromo-1H-benzotriazole in a yield of 9.48 g (90% yield). | [References]
[1] Organic and Biomolecular Chemistry, 2018, vol. 16, # 37, p. 6902 - 6907 [2] Patent: US2012/65191, 2012, A1. Location in patent: Page/Page column 26; 27 [3] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 5, p. 827 - 832 [4] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 20, p. 6832 - 6846 [5] Patent: KR2016/30566, 2016, A. Location in patent: Paragraph 0267-0270 |
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