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Thujyl alcohol, also known as α-thujone or α-thujanol, is a monoterpene alcohol derived from the essential oils of various plants, particularly from the Artemisia and Thuja genera. It is a colorless liquid with a strong, camphor-like odor and is known for its potential medicinal properties, such as antiseptic and anti-inflammatory effects. Thujyl alcohol is also used as a flavoring agent in food and beverages, as well as in the production of perfumes and cosmetics. However, it is important to note that thujyl alcohol can be toxic in high concentrations, and its use is regulated in many countries due to potential health risks, particularly when ingested or inhaled in large amounts.

513-23-5

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513-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 513-23-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 513-23:
(5*5)+(4*1)+(3*3)+(2*2)+(1*3)=45
45 % 10 = 5
So 513-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-6(2)10-4-8(10)7(3)9(11)5-10/h6-9,11H,4-5H2,1-3H3/t7-,8+,9+,10-/m1/s1

513-23-5Downstream Products

513-23-5Relevant academic research and scientific papers

(-) 3 Isothujone, a small nonnitrogenous molecule with antinociceptive activity in mice

Rice,Wilson

, p. 1054 - 1057 (2007/10/13)

(-) 3 isothujone and (+) 3 thujone were examined for antinociceptive activity using the hot plate and Nilsen tests. In the hot plate test (-) 3 isothujone (ED50 = 6.5 mg/kg) was found to be codeine like and equipotent with (-) Δ9 tetrahydrocannabinol while the racemic material was essentially half as potent as the levorotatory isomer. (+) 3 Thyjone was inactive in both antinociceptive tests as were several structural analogues of the 3 thujones. As with the THC's less antinociceptive activity was observed in the Nilsen test than in the hot plate assay. Acute toxicities for the 3 thujones were determined and vastly improved synthetic procedures have been developed for two long known but difficultly accessible 3 thujanols.

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