4,5-DIBROMO-1H-1,2,3-TRIAZOLE

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CAS:15294-81-2
Purity:99 Package:25KG
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CAS:15294-81-2
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Products Intro: Product Name:4,5-Dibromo-1H-1,2,3-triazole
CAS:15294-81-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-10275

4,5-DIBROMO-1H-1,2,3-TRIAZOLE manufacturers

4,5-DIBROMO-1H-1,2,3-TRIAZOLE Basic information
Product Name:4,5-DIBROMO-1H-1,2,3-TRIAZOLE
Synonyms:4,5-DIBROMO-1H-1,2,3-TRIAZOLE;1H-1,2,3-triazole, 4,5-dibromo-;4,5-dibromo-2H-1,2,3-triazole;4,5-dibromo-2H-triazole;4,5-Dibrom-1H-1,2,3-triazole;v-Triazole,4,5-dibroMo- (8CI);NSC222414;v-Triazole,4,5-dibroMo-
CAS:15294-81-2
MF:C2HBr2N3
MW:226.86
EINECS:
Product Categories:
Mol File:15294-81-2.mol
4,5-DIBROMO-1H-1,2,3-TRIAZOLE Structure
4,5-DIBROMO-1H-1,2,3-TRIAZOLE Chemical Properties
Melting point 194 °C (decomp)
Boiling point 47,3 C
density 2.18 g/cm
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Methanol
form powder to crystal
pka5.22±0.70(Predicted)
color White to Light yellow
InChIInChI=1S/C2HBr2N3/c3-1-2(4)6-7-5-1/h(H,5,6,7)
InChIKeyGUQUYKTWVBJKFL-UHFFFAOYSA-N
SMILESN1C(Br)=C(Br)N=N1
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
HS Code 2933.99.8290
HazardClass IRRITANT
MSDS Information
4,5-DIBROMO-1H-1,2,3-TRIAZOLE Usage And Synthesis
Uses4,5-Dibromo-1H-1,2,3-triazole is an intermediate used in preparation of isoxazole derivative herbicides.
Synthesis
1,2,3-1H-Triazole

288-36-8

4,5-DIBROMO-1H-1,2,3-TRIAZOLE

15294-81-2

Example 120: Preparation of 4,5-dibromo-1H-1,2,3-triazole. Bromine (1.5 mL, 29 mmol) was slowly added to a solution of 1H-[1,2,3]triazole (1.26 mL, 21.7 mmol) in water (10 mL) at 5 °C. The reaction mixture was stirred at 5°C for 1.5 h. The white solid (2.375 g) was isolated by filtration and washed with cold water (5 mL). Bromine (1.5 mL, 29 mmol) was added again to the combined filtrates. The mixture was stirred at room temperature for 20 h. More white solid (1.83 g) was separated by filtration and washed with cold water (5 mL). Bromine (1.5 mL, 29 mmol) was added a third time to the combined filtrates. The reaction mixture was stirred at room temperature for 20 h. Additional white solid (375 mg) was isolated by filtration and washed with cold water (5 mL). All white solids were combined and dried to give 4,5-dibromo-1H-[1,2,3]- triazole (4.92 g, 93% yield). Melting point: 194.7°C.

References[1] Journal of the Chemical Society - Perkin Transactions 1, 1996, # 12, p. 1341 - 1347
[2] Patent: WO2007/96576, 2007, A1. Location in patent: Example I20
[3] Patent: WO2017/80980, 2017, A1. Location in patent: Page/Page column 68-69
[4] Justus Liebigs Annalen der Chemie, 1947, vol. 558, p. 34,41
[5] Journal of the Chemical Society - Perkin Transactions 1, 1996, # 13, p. 1535 - 1543
4,5-DIBROMO-1H-1,2,3-TRIAZOLE Preparation Products And Raw materials
Raw materials1,2,3-TRIAZOLE-4-CARBOXYLIC ACID-->1,2,3-1H-Triazole
Preparation Products4,5-DibroMo-2-Methyl-2H-1,2,3-triazole
Tag:4,5-DIBROMO-1H-1,2,3-TRIAZOLE(15294-81-2) Related Product Information
4,5-DIBROMO-1H-1,2,3-TRIAZOLE