84227-78-1 Usage
Chemical structure
The compound consists of a benzimidazole group attached to a 1,2-propanediol molecule.
Benzimidazole group
A heterocyclic compound containing both nitrogen and carbon atoms in its ring structure, commonly found in pharmaceuticals and agricultural chemicals.
1,2-Propanediol
A type of alcohol often used as a solvent and in the production of various consumer products.
Potential applications
The combination of benzimidazole and 1,2-propanediol in this compound may have potential applications in the pharmaceutical or chemical industries.
Further research
More research is needed to fully understand the properties and uses of 1,2-Propanediol,3-(1H-benzimidazol-1-yl)-(9CI).
Molecular weight
The approximate molecular weight of the compound is 196.22 g/mol.
Appearance
The compound is likely to be a solid or a viscous liquid, depending on the specific conditions.
Solubility
The solubility of the compound in various solvents would depend on the properties of the benzimidazole and 1,2-propanediol moieties.
Stability
The stability of the compound under different conditions (e.g., temperature, pressure, and exposure to light) would need to be determined through further research.
Reactivity
The reactivity of the compound with other chemicals or under specific conditions would also need to be investigated.
Toxicity
The toxicity of the compound, if any, would need to be assessed through appropriate testing methods.
Environmental impact
The potential environmental impact of the compound, including its biodegradability and potential for bioaccumulation, would need to be evaluated.
Synthesis
The synthesis of 1,2-Propanediol,3-(1H-benzimidazol-1-yl)-(9CI) would involve the formation of a bond between the benzimidazole and 1,2-propanediol moieties, likely through a condensation reaction or other chemical process.
Purity
The purity of the synthesized compound would need to be confirmed through analytical techniques such as chromatography or spectroscopy.
Check Digit Verification of cas no
The CAS Registry Mumber 84227-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,2 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84227-78:
(7*8)+(6*4)+(5*2)+(4*2)+(3*7)+(2*7)+(1*8)=141
141 % 10 = 1
So 84227-78-1 is a valid CAS Registry Number.
84227-78-1Relevant articles and documents
Use of tosylated glycerol carbonate to access N-glycerylated aza-aromatic species
Vilkauskaite, Gyte,Krik?tolaityte, Sonata,Paliulis, Osvaldas,Rollin, Patrick,Tatibou?t, Arnaud,?a?kus, Algirdas
, p. 3721 - 3727 (2013/05/09)
Tosylated glycerol carbonate was used for N-glyceryl functionalization of diverse aza-aromatic systems. Depending on the pKa of the aza-heterocycle and the reaction conditions applied, original N-alkylated or N-acylated aza-heterocyclic derivat
Acyclic Analogs of Nucleosides. Synthesis of Hydroxyalkylbenzimidazoles and -Benzotriazoles
Yavorskii, A. E.,Stetsenko, A. V.,Zavgorodnii, S. G.,Florent'ev, V. L.
, p. 163 - 167 (2007/10/02)
Condensation of trimethylsilyl derivatives of benzimidazole and benzotriazole with alkylating agents in the presence of trimethylsilyl trifluoromethanesulfonate or SnCl4, or direct alkylation of the sodium salts of benzimidazole and benzotriazole, gives 1-(2,3-dihydroxypropyl)-, 1-(3-hydroxy-2-oxabutyl)-, 1-(3-hydroxymethyl-4-hydroxy-2-oxabutyl)-, and 1-(1,5-dihydroxy-3-oxapent-2-yl)benzimidazole and -benzotriazole.
