3296-50-2 Usage
Uses
Used in Chemical Synthesis:
Trans-hydrindane is used as a synthetic intermediate for the production of various chemicals, including pharmaceuticals, pesticides, and fragrances. Its ability to serve as a building block in the synthesis of complex organic molecules makes it valuable in the chemical industry.
Used in Flavoring and Fragrance Industry:
In the food industry, trans-hydrindane is used as a flavoring agent. Its mild, sweet odor contributes to the enhancement of flavors in various food products, providing a pleasant sensory experience for consumers.
Used in Personal Care Products:
Trans-hydrindane is also used as an additive in some personal care products, where it can contribute to the texture, stability, or scent of the formulations, ensuring a high-quality consumer experience.
Used in Oil and Gas Industry:
In the oil and gas sector, trans-hydrindane has applications as a surfactant, which helps in the extraction and processing of hydrocarbons. Its surfactant properties aid in the efficiency of oil recovery processes.
Used in Adhesives and Sealants Production:
Trans-hydrindane is utilized in the production of adhesives and sealants, where it enhances the bonding and sealing properties of these materials, making them more effective for various applications.
While trans-hydrindane is generally considered to have low toxicity, it is important to note that prolonged or high-level exposure can cause irritation to the skin, eyes, and respiratory system. Additionally, it may have harmful effects on aquatic organisms, highlighting the need for responsible handling and disposal in industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3296-50-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3296-50:
(6*3)+(5*2)+(4*9)+(3*6)+(2*5)+(1*0)=92
92 % 10 = 2
So 3296-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H16/c1-2-5-9-7-3-6-8(9)4-1/h8-9H,1-7H2/t8-,9-/m0/s1
3296-50-2Relevant academic research and scientific papers
Polyspiranes, 16. - Cascade Rearrangements, 11. - Synthesis, Structure, Conformation, and Dynamics of Heptacyclo1,5.05,9.09,13.013,17.017,21>tetracosane (Coronane)
Wehle, Detlef,Schormann, Norbert,Fitjer, Lutz
, p. 2171 - 2178 (2007/10/02)
Coronane (2) was synthesized by addition of allylmagnesium bromide to ketone 7, rearrangement of the resulting homoallyl alcohol 8a to diene 9, hydrozirconization of 9 followed by bromination to give 11, and finally radical cyclization of 11.A direct cyclization of 9 using tri(n-butyl)tin hydride failed. 2 is all-cis-configurated, adopts a chair conformation in the crystal state and in solution and exhibits an extremely low barrier of inversion (ΔG(excit.)173 /= 8.6 kcal/mol).
FORMATION OF SOME BICYCLIC SYSTEMS BY RADICAL RING-CLOSURE
Beckwith, Athelstan L. J.,Phillipou, George,Serelis, Algirdas K.
, p. 2811 - 2814 (2007/10/02)
The rates and stereochemistry of ring closure of the radicals (2), (9), (10), and (16) have been determined and rationalised.
