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84227-78-1

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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.

84227-78-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1H-benzimidazol-1-yl)propane-1,2-diol

1.2 Other means of identification

Product number -
Other names 3-Benzoimidazol-1-yl-propane-1,2-diol

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:84227-78-1 SDS

84227-78-1Downstream Products

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.

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