1592-61-6 Usage
Molecular Weight
211.28 g/mol The relative molecular mass of the compound based on the atomic weights of its constituent elements.
Structure
Carbazole ring with a hydroxyl group at position 1 and a methyl group at position 9 The compound's core structure is a carbazole ring, which is a tricyclic aromatic system with a nitrogen atom in the middle ring. The hydroxyl group is attached to the first position, and the methyl group is at the ninth position.
Classification
Tertiary alcohol The compound is classified as a tertiary alcohol because the hydroxyl group (-OH) is attached to a carbon atom that is bonded to three other carbon atoms.
Derivative of Carbazole
A heterocyclic aromatic compound The compound is derived from carbazole, which is a heterocyclic aromatic compound consisting of a tricyclic ring system with a nitrogen atom in the middle ring.
Potential Applications
Organic synthesis, dyes, pigments, and pharmaceuticals The compound has potential uses in the synthesis of organic compounds, as well as in the production of dyes, pigments, and pharmaceuticals due to its unique structure and properties.
Research and Development
Interesting target for various industries The unique structure and properties of 1H-Carbazol-1-ol, 2,3,4,9-tetrahydro-9-methylmake it an interesting target for further research and development in different industries, such as chemical, pharmaceutical, and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 1592-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1592-61:
(6*1)+(5*5)+(4*9)+(3*2)+(2*6)+(1*1)=86
86 % 10 = 6
So 1592-61-6 is a valid CAS Registry Number.
1592-61-6Relevant academic research and scientific papers
Arnould, J.C.,Cossy, J.,Pete, J.P.
, p. 1585 - 1592 (1980)
The photochemical behaviour of 2-alkylamino 2-cyclohexenones is very sensitive to the nitrogen substituents. α-Ketoazetidines are produced by irradiation of 2-methanesulfonamido-2-cyclohexenones; however a desulfonation and aryl migration process can complete in the case of 2-arenesulfonamido-2-cyclohexenones.Furthermore divinylamine and photo-Fries rearrangements are the main reactions with 2-anilino 2-cyclohexenone and 2-benzoylamido 2-cyclohexenone respectively.
