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2034-22-2

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2034-22-2 Usage

General Description

2,4,5-Tribromoimidazole(2,4,5-TBI) on condensation with sugar precursors yields 2,4,5-TBI nucleosides.

Biochem/physiol Actions

2,4,5-Tribromoimidazole induces poisoning typical of uncouplers of oxidative phosphorylation in rats.

Check Digit Verification of cas no

The CAS Registry Mumber 2034-22-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2034-22:
(6*2)+(5*0)+(4*3)+(3*4)+(2*2)+(1*2)=42
42 % 10 = 2
So 2034-22-2 is a valid CAS Registry Number.
InChI:InChI=1/2C3H2Br3N2.Cd/c2*4-1-2(5)8-3(6)7-1;/h2*3,7H;/q2*-1;+2

2034-22-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L05716)  2,4,5-Tribromoimidazole, 97%   

  • 2034-22-2

  • 5g

  • 351.0CNY

  • Detail
  • Alfa Aesar

  • (L05716)  2,4,5-Tribromoimidazole, 97%   

  • 2034-22-2

  • 25g

  • 1258.0CNY

  • Detail
  • Aldrich

  • (141704)  2,4,5-Tribromoimidazole  97%

  • 2034-22-2

  • 141704-25G

  • 1,378.26CNY

  • Detail

2034-22-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,5-tribromo-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2,4,5-TribroMoiMidazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2034-22-2 SDS

2034-22-2Relevant articles and documents

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Linda

, p. 3297 (1969)

-

Synthesis, anti-HIV-1 and antiproliferative evaluation of novel 4-nitroimidazole derivatives combined with 5-hydroxy-4-pyridinone moiety

Shirvani, Pouria,Fassihi, Afshin,Saghaie, Lotfollah,Van Belle, Siska,Debyser, Zeger,Christ, Frauke

, (2019/11/26)

In an effort to synthesize more effective non-nucleoside reverse transcriptase inhibitors (NNRTIs) against the HIV-1 infection, a new series of novel 4-nitroimidazole derivatives combined with 5-hydroxy-4-pyridinone moiety were designed by molecular docking studies, prepared and characterized by spectroscopic techniques. All the synthesized compounds were in vitro evaluated for their inhibitory effect against the HIV-1 replication in the MT-4 cells. Results showed that none of these synthesized compounds displayed any specific anti HIV-1 activity. Surprisingly, these compounds showed high cytotoxicity against MT-4 cells with low selectivity index (50 = 1.3 μM and EC50 = 1.8 μM respectively).

Syntheses, Structural Characterization, Reactivity, and Theoretical Studies on Some Heteroligand Oxoperoxotungstate(VI)

Das, Nandita,Chowdhury, Shubhamoy,Dutta Purkayastha, Ranendra N.

, p. 43 - 54 (2017/01/17)

White microcrystalline diamagnetic oxoperoxotungstate(VI) complexes K[WO(O2)2F]·H2O, K2[WO(O2)2(CO3)]·H2O, [WO(O2)(SO4)(H2O)2] have been synthesized from reaction of Na2WO4·2H2O with aqueous HF, solid KHCO3, aqueous H2SO4 (W:F? 1:3; W: CO3 2 ? 1:1; and W: SO4 2 ? 1:3), and an excess of 30% H2O2 at pH 7.5–8. Precipitation was completed by the addition of precooled acetone. The occurrence of terminal W?O and triangular bidentate O2 2 ?(C 2 v) in the synthesized compounds was ascertained from IR spectra. The IR spectra also suggested that the F? and SO4 2 ? ions in K[WO(O2)2F]·H2O and [WO(O2)(SO4)(H2O)2] were bonded to the WO +4 center in monodentate manner, while CO3 2 ? ion in K2[WO(O2)2(CO3)]·H2O binds the metal center in bidentate chelating fashion. The complex [WO(O2)(SO4)(H2O)2] is stable upto 110°C. The water molecule in [WO(O2)(SO4)(H2O)2] is coordinated to the WO +4 center, whereas it occurs as water of crystallization in the corresponding peroxo(fluoro) and peroxo(carbonato) compounds. Mass spectra of the compounds are in good agreement with the molecular formulae of the complexes. K2[WO(O2)2(CO3)]·H2O acts as an oxidant for bromide in the aqueous-phase bromination of organic substrates to the corresponding bromo-organics, and the complex also oxidizes Hantzsch-1,4-dihydropyridine to the corresponding pyridine derivative in excellent yield at room temperature. Density functional theory computation was carried out to compute the frequencies of relevant vibrational modes and electronic properties, and the results are in agreement with the experimentally obtained data.

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