6290-20-6 Usage
General Description
2-hexyl-1,3-dioxane is a chemical compound with the molecular formula C10H20O2. It is a type of dioxane, which is a class of organic compounds with a six-membered ring containing two oxygen atoms. The 2-hexyl-1,3-dioxane is commonly used in the production of cosmetic and personal care products, such as perfumes and lotions, as well as in the formulation of various industrial and household cleaners. It is important to handle this chemical with care, as it may cause irritation to the skin, eyes, or respiratory system if not properly managed. It is also recommended to use this chemical in well-ventilated areas and to wear personal protective equipment, such as gloves and goggles, when handling it. Overall, 2-hexyl-1,3-dioxane is a versatile compound with various applications, but it should be used responsibly to avoid any health and safety risks.
Check Digit Verification of cas no
The CAS Registry Mumber 6290-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6290-20:
(6*6)+(5*2)+(4*9)+(3*0)+(2*2)+(1*0)=86
86 % 10 = 6
So 6290-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O2/c1-2-3-4-5-7-10-11-8-6-9-12-10/h10H,2-9H2,1H3
6290-20-6Relevant articles and documents
Facile SN' Reaction of Alkyl-lithiums with 2-Vinyl-1,3-dioxane
Bailey, William F.,Zartun, Donna L.
, p. 34 - 35 (1984)
Treatment of 2-vinyl-1,3-dioxane with n-, s-, or t-butyl-lithium in diethyl ether or n-pentane solution results in facile nucleophilic addition of RLi to the carbon-carbon double bond with concomitant cleavage of the ring C-O bond (SN' process) to give high yields of enol ethers having the structure HO3OCH=CHCH2R.
Copper nanoparticle-catalyzed cross-coupling of alkyl halides with Grignard reagents
Kim, Ju Hyun,Chung, Young Keun
supporting information, p. 11101 - 11103 (2013/11/19)
A cross-coupling reaction between alkyl bromides and chlorides and various Grignard reagents was carried out in the presence of commercially available copper or copper oxide nanoparticles as a catalyst and an alkyne additive. The catalytic system shows high activity, a broad scope, and good functional group tolerance.
Nickel-catalyzed cross-coupling of non-activated and functionalized alkyl halides with alkyl grignard reagents
Vechorkin, Oleg,Hu, Xile
supporting information; experimental part, p. 2937 - 2940 (2009/09/08)
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