ChemicalBook--->CAS DataBase List--->32046-62-1

32046-62-1

32046-62-1 Structure

32046-62-1 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280-P301+P310-P260
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

5-BROMO-1H-BENZOTRIAZOLE(32046-62-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Bromo-1,2-benzenediamine

1575-37-7

5-BROMO-1H-BENZOTRIAZOLE

32046-62-1

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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