2,4,5-Tribromo-1H-imidazole | CAS No. 2034-22-2

2,4,5-Tribromo-1H-imidazole

Basic Information

CAS Number

2034-22-2

Molecular Formula

C3HBr3N2

Molecular Weight

304.77 g/mol

AD

Basic Physical Properties

Melting Point

212°C

Boiling Point

401.3 °C at 760 mmHg

Flash Point

196.5 °C

Refractive Index

1.6500 (estimate)

C1(=C(N=C(N1)Br)Br)Br

InChI

InChI=1S/C3HBr3N2/c4-1-2(5)8-3(6)7-1/h(H,7,8)

InChIKey

JCGGPCDDFXIVQB-UHFFFAOYSA-N

LogP

2.6972

Topological Polar Surface Area

28.68 Ų

Hydrogen Bond Donor/Acceptor

1 / 2

Complexity

88.6

Safety Information

View Safety Information

GHS Hazard Pictograms

H300H300
H311H311
H315H315
H319H319
H331H331
H335H335

Hazard Statement

H300 Fatal if swallowed
Acute toxicity, oral
H311 Toxic in contact with skin
Acute toxicity, dermal
H315 Causes skin irritation
Skin corrosion/irritation
H319 Causes serious eye irritation
Serious eye damage/eye irritation
H331 Toxic if inhaled
Acute toxicity, inhalation
H335 May cause respiratory irritation
Specific target organ toxicity, single exposure; Respiratory tract irritation

Hazard Class

Class 6.1 Class 6.1

Sensitiveness

Sensitive to air and light

Synonyms & References

English

  • AM20090155
  • Imidazole,4,5-tribromo-
  • 2,4,5-tribromo-imidazole
  • T2266
  • 2,4,5-Tribromoimidazole, 97%
  • NSC-514965
  • W-107629
  • DTXSID2022173
  • SCHEMBL69879
  • BRN 0115314
  • NS00026589
  • EINECS 217-997-5
  • CL2210
  • AI3-62059
  • CHEMBL363992
  • 2034-22-2
  • MFCD00005184
  • Q27893870
  • AC-7522
  • 2,4,5-tribromo imidazole
  • Tribromoimidazole
  • NSC514965
  • 2,4,5-TRIBROMOIMIDAZOLE
  • 2,5-Tribromoimidazole
  • FT-0609785
  • EN300-140762
  • AC-907/25014002
  • Z1269217056
  • AS-15002
  • NSC 514965
  • 1H-Imidazole, 2,4,5-tribromo-

MDL Number

MFCD00005184

FAQ

What are the physical and chemical properties of 2,4,5-Tribromo-1H-imidazole (CAS: 2034-22-2)?

2,4,5-Tribromo-1H-imidazole (CAS: 2034-22-2) is a white crystalline solid with a molecular weight of approximately 324.02 g/mol. It has a low solubility in water but is more soluble in organic solvents. The compound is moderately reactive, showing some tendencies to undergo substitution reactions.

How is 2,4,5-Tribromo-1H-imidazole (CAS: 2034-22-2) typically synthesized?

2,4,5-Tribromo-1H-imidazole is typically synthesized through the bromination of 1H-imidazole using bromine in the presence of a suitable catalyst. The reaction is selective and yields a pure product with high efficiency.

What industries use 2,4,5-Tribromo-1H-imidazole (CAS: 2034-22-2)?

2,4,5-Tribromo-1H-imidazole is utilized in several industries, including pharmaceuticals for its antimicrobial properties, and in the synthesis of organic compounds. It is also used in the production of sensors and as a precursor in semiconductor manufacturing.

What precautions should be taken when handling 2,4,5-Tribromo-1H-imidazole (CAS: 2034-22-2)?

Proper handling of 2,4,5-Tribromo-1H-imidazole requires the use of personal protective equipment (PPE) such as gloves, goggles, and a lab coat. The compound should be stored in a fume hood and handled in a well-ventilated area to avoid inhalation. In case of a spill, immediately clean it up with appropriate absorbent materials and ensure proper disposal. Always refer to the Safety Data Sheet (SDS) for detailed information.

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