7767-16-0 Usage
Chemical Structure
A benzimidazole ring system with a phenyl group and an ethyl ester functional group
Usage
Intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds
Potential Applications
Medicine, specifically in the development of drugs with antifungal, antibacterial, and anti-inflammatory properties
Industry Relevance
Valuable compound in the pharmaceutical and chemical industries due to its versatile properties and potential therapeutic applications
Functional Groups
Benzimidazole ring, phenyl group, and ethyl ester
Molecular Weight
Approximately 251.3 g/mol
Appearance
Likely a solid or crystalline substance, though specific appearance may vary depending on conditions
Solubility
Solubility information not provided, but generally, similar compounds are soluble in organic solvents like ethanol, methanol, or acetone
Stability
Stability information not provided, but generally, similar compounds are stable under normal temperature and pressure conditions
Reactivity
Reactivity information not provided, but generally, ester functional groups can undergo hydrolysis reactions to form carboxylic acids and alcohols
Synthesis
Typically synthesized through the reaction of a benzimidazole-2-acetic acid derivative with an appropriate phenyl compound and an alcohol, such as ethanol, in the presence of an acid catalyst
Purity
Purity information not provided, but high purity is often required for pharmaceutical and chemical applications
Safety and Handling
Safety and handling information not provided, but it is important to follow proper laboratory safety protocols when working with 1H-Benzimidazole-2-acetic acid, 1-phenyl-, ethyl ester, including the use of personal protective equipment and handling in a well-ventilated area or fume hood
Check Digit Verification of cas no
The CAS Registry Mumber 7767-16-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,6 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7767-16:
(6*7)+(5*7)+(4*6)+(3*7)+(2*1)+(1*6)=130
130 % 10 = 0
So 7767-16-0 is a valid CAS Registry Number.
7767-16-0Relevant articles and documents
Acetohydroxamic acids
-
, (2008/06/13)
The invention provides new acetohydroxamic acid derivatives, having interesting properties on the central nervous system, of the formula: R1 R2 R3 C-CO-NHOH, in which R2 and R3 are each hydrogen or C1-6 alkyl, and R1 is C1-6 alkyl Z1 Z2 N (where Z1 and Z2 are each phenyl, substituted phenyl, or cycloalkyl), substituted hydantoinyl, benzhydroxylcarboxamido, Z3 CH2 -- (where Z3 = optionally substituted aryl), Z4 -A- (where Z4 is optionally substituted phenyl or naphthyl, and A is --NH--, --N(C1-4 alkyl)--, --N(C5-6 cycloalkyl)--, --NHCO--, --N(C1-4 alkyl)CO--, --N(C5-6 cycloalkyl)CO--, --CONH--, --CON(C1-4 alkyl)--, --CON(C5-6 cycloalkyl)--, --NHCONH--, --N(C5 H6)CONH--, or --N(substituted phenyl)CONH--, optionally substituted benzimidazolyl, or an optionally substituted tricyclic radical, and their metal and acid addition salts.
