82010-90-0 Usage
Physical state
Colorless liquid
The compound appears as a colorless liquid, which indicates its lack of color and its ability to flow.
Strong odor
2-[(3-methylbut-3-enyl)thio]ethanol has a noticeable and intense smell, which contributes to its use as a fragrance and flavoring agent.
Common uses
Fragrances, flavoring agents, antimicrobial, and antibacterial properties
The compound is widely used in perfumes, cosmetics, household cleaning products, and personal care items due to its pleasant scent and ability to inhibit the growth of microbes and bacteria.
Industrial applications
Solvent, stabilizer
In various industrial processes, 2-[(3-methylbut-3-enyl)thio]ethanol serves as a solvent, helping to dissolve other substances, and as a stabilizer, improving the stability of products.
Health concerns
Skin irritation, respiratory issues
Prolonged or excessive exposure to the compound may lead to skin irritation, respiratory problems, and other health concerns, emphasizing the need for proper handling and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 82010-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,1 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82010-90:
(7*8)+(6*2)+(5*0)+(4*1)+(3*0)+(2*9)+(1*0)=90
90 % 10 = 0
So 82010-90-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H14OS/c1-7(2)3-5-9-6-4-8/h8H,1,3-6H2,2H3
82010-90-0Relevant academic research and scientific papers
Studies on the Use of Bidentate Ligands in the Directed Pauson-Khand Reaction
Krafft, Marie E.,Juliano, Carmelinda A.
, p. 5106 - 5115 (2007/10/02)
The use of bidentate ligands in the directed Pauson-Khand reaction was investigated.Substrates with a three-carbon linkage between the two heteroatoms gave better results than substrates containing two-carbon tethers.Higher yields and better regioselectivities were observed with thioamines and bisthioethers compared to diamines.Overall, only a few bidentate substrates showed marked improvements over previous results obtained with analogous monodentate compounds.Rationalizations based on the possible modes of cycloaddition operative for the various substrates studied are presented.
