194209-32-0 Usage
Chemical Class
Phenols
Explanation
1,2-Benzenediol, 4-[2-(1H-pyrrol-1-yl)ethyl](9CI) belongs to the class of phenols, which are aromatic compounds containing one or more hydroxyl groups attached to a benzene ring.
Explanation
This is an alternative name for the compound, which highlights the presence of a pyrrole ring and a phenol group in its structure.
Explanation
The compound is derived from benzene, with two hydroxyl groups (-OH) attached to adjacent carbon atoms, and a pyrrole ring, which is a heterocyclic organic compound.
Explanation
The compound contains two hydroxyl groups and a pyrrole ring, which are its main functional groups that contribute to its chemical properties and reactivity.
Explanation
Due to its unique structure, 1,2-Benzenediol, 4-[2-(1H-pyrrol-1-yl)ethyl](9CI) may have various applications in different industries, such as pharmaceuticals, dyes, and other industrial processes.
Explanation
The reactivity of the compound with other chemicals would depend on its specific chemical structure and characteristics, which can influence its potential applications and uses.
Explanation
Based on the provided information, the molecular formula can be inferred as C11H12O2N, which includes carbon, hydrogen, oxygen, and nitrogen atoms in its structure.
Explanation
The molecular weight can be calculated from the molecular formula, which in this case is approximately 192 g/mol.
Explanation
Phenolic compounds are generally solids or liquids at room temperature, depending on their molecular weight and structure.
Explanation
Phenolic compounds are typically soluble in organic solvents like ethanol, methanol, or acetone, and may have limited solubility in water due to the presence of hydroxyl groups.
Structure
Benzene derivative with two hydroxyl groups and a pyrrole ring
Functional Groups
Hydroxyl groups, pyrrole ring
Applications
Pharmaceuticals, dyes, and industrial processes
Chemical Reactivity
Depends on specific structure and characteristics
Molecular Weight
Approximately 192 g/mol (tentative)
Physical State
Likely a solid or liquid at room temperature
Solubility
Soluble in organic solvents, may be slightly soluble in water
Check Digit Verification of cas no
The CAS Registry Mumber 194209-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,2,0 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 194209-32:
(8*1)+(7*9)+(6*4)+(5*2)+(4*0)+(3*9)+(2*3)+(1*2)=140
140 % 10 = 0
So 194209-32-0 is a valid CAS Registry Number.
194209-32-0Relevant articles and documents
Attempts to mimic key bond-forming events associated with the proposed biogenesis of the pentacyclic lamellarins
Axford, Lorraine C.,Holden, Kate E.,Hasse, Katrin,Banwell, Martin G.,Steglich, Wolfgang,Wagler, Joerg,Willis, Anthony C.
, p. 80 - 93 (2008/04/04)
The pyrrole-tethered veratroles 16 and 27 each engage in PIFA-induced oxidative cyclization reactions to give compounds 22 and 29, respectively, which incorporate a key tricyclic fragment associated with the title natural products. In contrast, the corresponding catechols 11 and 12 only produce polymeric materials on subjection to analogous reaction conditions. Efforts to study lactone ring formation by the oxidative cyclization of catechol 30 and veratrole 38 have been thwarted by an inability to prepare the former substrate and decomposition of the latter. The reported conversions 44 ? 45 and 46 ? 47 suggest that a C2-carboxy group attached to the pyrrole ring can ?direct' the oxidative cyclization of N-tethered aryl groups. The acquisition of compound 22 by the means described herein provides an adventitious and concise route to the racemic modification of the pyrrolo[2,1-a]isoquinoline alkaloid crispine A (52). CSIRO 2008.
