ChemicalBook--->CAS DataBase List--->1753-75-9

1753-75-9

1753-75-9 Structure

1753-75-9 Structure
IdentificationBack Directory
[Name]

5-BROMO-2,1,3-BENZOTHIADIAZOLE
[CAS]

1753-75-9
[Synonyms]

BUTTPARK 95\50-70
5-BROMO-2,1,3-BENZOTHIADIAZOLE
5-BROMO-BENZO[1,2,5]THIADIAZOLE
5-Bromo-benzo[2,1,3]thiadiazole
2,1,3-Benzothiadiazole, 5-bromo-
5-Bromobenzo[c][1,2,5]thiadiazole
[Molecular Formula]

C6H3BrN2S
[MDL Number]

MFCD00460091
[MOL File]

1753-75-9.mol
[Molecular Weight]

215.07
Chemical PropertiesBack Directory
[Melting point ]

51-53°C
[Boiling point ]

272.2±13.0 °C(Predicted)
[density ]

1.859±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

Solid
[pka]

-0.73±0.36(Predicted)
[Appearance]

Light brown to gray Solid
[InChI]

1S/C6H3BrN2S/c7-4-1-2-5-6(3-4)9-10-8-5/h1-3H
[InChIKey]

LLCRUZDFDGTAAN-UHFFFAOYSA-N
[SMILES]

Brc1ccc2nsnc2c1
[CAS DataBase Reference]

1753-75-9
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

36/37/38-36-22
[Safety Statements ]

26-36/37/39-37/39
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Spectrum DetailBack Directory
[Spectrum Detail]

5-BROMO-2,1,3-BENZOTHIADIAZOLE(1753-75-9)1HNMR
5-BROMO-2,1,3-BENZOTHIADIAZOLE(1753-75-9)FT-IR
Hazard InformationBack Directory
[Synthesis]

4-Bromo-1,2-benzenediamine

1575-37-7

5-BROMO-2,1,3-BENZOTHIADIAZOLE

1753-75-9

Example 2 Synthesis of 5-bromo-2,1,3-benzothiadiazole: A reaction mixture was prepared by mixing 4.0 g (21 mmol) of 4-bromophthalimide, 14 mL of thionyl chloride and 0.62 mL of concentrated sulfuric acid. The mixture was heated to reflux for 1 hour. Upon completion of the reaction, the mixture was cooled and subsequently slowly poured into ice water. The precipitate precipitated was collected by filtration and washed with plenty of water until the washings were neutral. Finally, the precipitate was thoroughly dried to give 4.5 g of 5-bromo-2,1,3-benzothiadiazole crude product (melting point 48 to 50 °C, yield 96.5%).

[References]

[1] RSC Advances, 2016, vol. 6, # 71, p. 66978 - 66989
[2] Patent: US2009/149676, 2009, A1. Location in patent: Page/Page column 5
[3] ChemMedChem, 2018, vol. 13, # 21, p. 2332 - 2348
[4] Chemistry of Heterocyclic Compounds (New York, NY, United States), 1967, vol. 3, p. 662 - 666
[5] Khimiya Geterotsiklicheskikh Soedinenii, 1967, vol. 3, # 5, p. 839 - 844
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