100017-18-3 Usage
General Description
"(2R,6R)-2-tert-butyl-6-methyl-1,3-dioxan-4-one" is a chemical compound with a molecular formula of C10H18O2. It is a cyclic ketone that is commonly used as a building block in organic synthesis. (2R,6R)-2-TERT-BUTYL-6-METHYL-1,3-DIOXAN-4-ONE is known for its ability to undergo a variety of chemical reactions, making it useful in the production of a wide range of different substances. It is also used as a flavoring agent in the food industry, adding a sweet, fruity, and slightly floral aroma and taste to various products. In addition to these applications, (2R,6R)-2-tert-butyl-6-methyl-1,3-dioxan-4-one has potential applications in pharmaceuticals, agrochemicals, and cosmetics due to its versatile reactivity and favorable odor profile.
Check Digit Verification of cas no
The CAS Registry Mumber 100017-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,1 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100017-18:
(8*1)+(7*0)+(6*0)+(5*0)+(4*1)+(3*7)+(2*1)+(1*8)=43
43 % 10 = 3
So 100017-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O3/c1-6-5-7(10)12-8(11-6)9(2,3)4/h6,8H,5H2,1-4H3/t6-,8-/m1/s1
100017-18-3Relevant articles and documents
Absolute configurations of melanoxadin, MR-93A, melanoxazal, and MR-93B
He, Tian-Jun,Zhu, Shijun,Lu, Xiao-Wei,Wu, Yikang,Li, Yan
, p. 647 - 654 (2015/01/30)
Fungal metabolites melanoxadin, MR-93A, melanoxazal, and MR-93B were synthesized with the key stereogenic centers derived from commercially available chiral building blocks. The optically active synthetic products with well-defined absolute configurations provided authentic samples for the stereoisomers of these oxazole-containing natural products and thus allowed for unambiguous assignments of their relative and absolute configurations. The large discrepancies in the optical rotations between the natural and the pure synthetic samples are discussed. Some errors in the previously reported NMR signal assignments are also corrected.
Optisch aktive Alkohole aus 1,3-Dioxan-4-onen; eine praktikable Variante der asymmetrischen Synthese unter nucleophiler Substitution an Acetalzentren
Seebach, Dieter,Imwinkelried, Rene,Stucky, Gerhard
, p. 182 - 183 (2007/10/02)
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