29279-82-1 Usage
Structure
Cyclobutanol derivative with three phenyl groups attached to the cyclobutanol ring
Physical state at room temperature
Colorless solid
Solubility
Insoluble in water
Uses
Primarily used in organic synthesis and as a building block for the preparation of more complex organic compounds
Potential applications
Pharmaceutical and material science research, catalysis, and as a chiral building block in organic chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 29279-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,7 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29279-82:
(7*2)+(6*9)+(5*2)+(4*7)+(3*9)+(2*8)+(1*2)=151
151 % 10 = 1
So 29279-82-1 is a valid CAS Registry Number.
29279-82-1Relevant academic research and scientific papers
Acid-catalyzed rearrangement of cyclobutanols. Syntheses of chrysenes, cyclopentenophenanthrenes, and diarylmethanes
Lee-Ruff, Edward,Hopkinson, Alan C.,Kazarians-Moghaddam, Hira,Gupta, Brij,Katz, Morris
, p. 154 - 159 (2007/10/02)
Acid-catalyzed reactions of 8-aryl or 8,8-diarylbicyclooct-2-en-7-ols lead to tetrahydrophenanthrene derivatives.For example 8-(1-naphthyl)-bicyclooct-2-en-7-ols give substituted chrysenes in methanesulphonic acid.In the case of the homologous 7-aryl or 7,7-diarylbicyclohept-2-en-6-ols a novel transformation of diarylmethanes is observed.A mechanism is proposed which accounts for the product distribution observed in these rearrangements.
