185949-58-0 Usage
Structure
A derivative of benzimidazole with a chloro and a methyl group
Potential Applications
Pharmaceutical industry, synthesis of various drugs
Safety Precautions
Handle with caution, follow proper safety protocols in laboratory settings
Research
Further research may be conducted to explore potential uses and properties
Chemical Classification
Organic compound, heterocyclic compound
Functional Groups
Amine, chloro, and methyl groups
Physical State
Likely a solid at room temperature (based on molecular size and complexity)
Solubility
Solvent compatibility not provided, but likely soluble in organic solvents (e.g., methanol, ethanol, or dimethyl sulfoxide) due to its molecular structure
Stability
Stability information not provided, but generally stable under normal laboratory conditions
Reactivity
Reactivity information not provided, but may react with strong acids, bases, or nucleophiles due to the presence of amine and chloro groups
Purity
Purity information not provided, but typically synthesized and used in a pure form for pharmaceutical applications
Synthesis
Synthesis method not provided, but likely involves chemical reactions with benzimidazole derivatives and appropriate reagents to introduce the chloro and methyl groups
Analysis
Analytical techniques such as nuclear magnetic resonance (NMR), mass spectrometry (MS), and infrared (IR) spectroscopy can be used to confirm its structure and purity
Check Digit Verification of cas no
The CAS Registry Mumber 185949-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,9,4 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 185949-58:
(8*1)+(7*8)+(6*5)+(5*9)+(4*4)+(3*9)+(2*5)+(1*8)=200
200 % 10 = 0
So 185949-58-0 is a valid CAS Registry Number.
185949-58-0Relevant articles and documents
Carboxylic acid amides, the preparation thereof, and their use as pharmaceutical compositions
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, (2008/06/13)
The present invention relates to new substituted carboxylic acid amides of general formula wherein A, B and R1 to R5 are defined as in claim 1, the tautomers, the enantiomers, the diastereomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, which have valuable properties. The compounds of the above general formula I as well as the tautomers, the enantiomers, the diastereomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, and their stereoisomers have valuable pharmacological properties, particularly an antithrombotic activity and a factor Xa-inhibiting activity.
NOVEL CARBOXAMIDES, THE PRODUCTION AND USE THEREOF AS MEDICAMENTS
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Page/Page column 147-148, (2010/02/07)
The invention relates to novel substituted carboxamides of general formula (I), in which A, B and R1 to R5 are as defined in claim 1, the tautomers, enantiomers, diastereomers, mixtures and salts thereof, in particular the physiologi
