38005-82-2 Usage
Uses
Used in Organic Synthesis:
Indan-1,5-diol is used as a starting material for the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Its presence of two hydroxyl groups makes it a versatile building block in the creation of a wide range of chemical products.
Used in Dye and Pigment Production:
Indan-1,5-diol is used as a key component in the production of dyes and pigments. Its chemical properties contribute to the color and stability of these products, making it an essential ingredient in this industry.
Used in Material Development:
Indan-1,5-diol has potential applications in the development of new materials. Its unique structure and properties can be leveraged to create innovative materials with specific characteristics for various applications.
Used as a Reagent in Chemical Reactions:
Indan-1,5-diol is used as a reagent in various chemical reactions. Its ability to participate in a range of chemical processes makes it a useful tool for chemists in research and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 38005-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,0 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38005-82:
(7*3)+(6*8)+(5*0)+(4*0)+(3*5)+(2*8)+(1*2)=102
102 % 10 = 2
So 38005-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O2/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5,9-11H,1,4H2
38005-82-2Relevant academic research and scientific papers
A photo-favorskii ring contraction reaction: The effect of ring size
Kammath, Viju Balachandran,?olomek, Tomá?,Ngoy, Bokolombe Pitchou,Heger, Dominik,Klán, Petr,Rubina, Marina,Givens, Richard S.
, p. 1718 - 1729 (2013/03/29)
The effect of ring size on the photo-Favorskii induced ring-contraction reaction of the hydroxybenzocycloalkanonyl acetate and mesylate esters (7a-d, 8a-c) has provided new insight into the mechanism of the rearrangement. By monotonically decreasing the ring size in these cyclic derivatives, the increasing ring strain imposed on the formation of the elusive bicyclic spirocyclopropanone 20 results in a divergence away from rearrangement and toward solvolysis. Cycloalkanones of seven or eight carbons undergo a highly efficient photo-Favorskii rearrangement with ring contraction paralleling the photochemistry of p-hydroxyphenacyl esters. In contrast, the five-carbon ring does not rearrange but is diverted to the photosolvolysis channel avoiding the increased strain energy that would accompany the formation of the spirobicyclic ketone, the "Favorskii intermediate 20". The six-carbon analogue demonstrates the bifurcation in reaction channels, yielding a solvent-sensitive mixture of both. Employing a combination of time-resolved absorption measurements, quantum yield determinations, isotopic labeling, and solvent variation studies coupled with theoretical treatment, a more comprehensive mechanistic description of the rearrangement has emerged.
