795296-17-2 Usage
Chemical structure
A benzimidazole ring with a carboxylic acid group, a trichloromethyl group, and a methyl ester functional group attached to it.
Molecular weight
Approximately 270.5 g/mol
Functional groups
Carboxylic acid, trichloromethyl, and methyl ester
Appearance
A solid or crystalline compound
Solubility
Soluble in organic solvents such as ethanol, methanol, and dichloromethane
Reactivity
The trichloromethyl group contributes to the compound's reactivity, making it a potential precursor for other chemical derivatives
Industrial and laboratory applications
Used as a building block in the synthesis of pharmaceuticals and agrochemicals
Synthesis
The compound can be synthesized through various methods, such as the reaction of a benzimidazole derivative with a chloroform reagent in the presence of a base
Stability
Generally stable under normal laboratory conditions, but sensitive to heat, light, and moisture
Safety precautions
Handle with care, as it may be toxic or harmful if inhaled, ingested, or absorbed through the skin. Use appropriate personal protective equipment (PPE) and follow proper disposal procedures
Storage
Store in a cool, dry, and well-ventilated area, away from heat, light, and sources of ignition
Regulatory status
Depending on the jurisdiction, 1H-Benzimidazole-4-carboxylic acid, 2-(trichloromethyl)-, methyl ester may be subject to specific regulations and guidelines for its use, handling, and disposal
Environmental impact
As with any chemical compound, proper disposal and handling are essential to minimize potential environmental impact
Potential hazards
May pose a risk of irritation to the eyes, skin, and respiratory system, as well as potential hazards if ingested or absorbed through the skin
Analytical techniques
Techniques such as nuclear magnetic resonance (NMR), infrared (IR) spectroscopy, and mass spectrometry (MS) can be used to analyze and confirm the structure of the compound
Purity
The purity of the compound can be determined using various analytical methods, such as high-performance liquid chromatography (HPLC) or gas chromatography (GC)
Synthesis scale
The synthesis of 1H-Benzimidazole-4-carboxylic acid, 2-(trichloromethyl)-, methyl ester can be carried out on a small scale in a laboratory or on a larger scale in an industrial setting, depending on the desired application and quantity needed
Derivatives
The compound can be further modified or functionalized to create a variety of derivatives with different properties and applications
Research interest
Due to its potential applications in pharmaceuticals and agrochemicals, 1H-Benzimidazole-4-carboxylic acid, 2-(trichloromethyl)-, methyl ester may be of interest to researchers in the fields of medicinal chemistry, chemical biology, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 795296-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,5,2,9 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 795296-17:
(8*7)+(7*9)+(6*5)+(5*2)+(4*9)+(3*6)+(2*1)+(1*7)=222
222 % 10 = 2
So 795296-17-2 is a valid CAS Registry Number.
