5048-30-6 Usage
General Description
7-Acetoxy-1-heptene is a chemical compound with the molecular formula C9H16O2. It is a clear, colorless liquid with a fruity odor. 7-ACETOXY-1-HEPTENE is used as a building block in the synthesis of various organic compounds and is also used as a fragrance ingredient in the production of perfumes and other personal care products. 7-Acetoxy-1-heptene is a highly reactive compound and should be handled with caution due to its potential for causing skin and eye irritation. It is also flammable and should be stored and handled in a well-ventilated area with proper safety precautions.
Check Digit Verification of cas no
The CAS Registry Mumber 5048-30-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,4 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5048-30:
(6*5)+(5*0)+(4*4)+(3*8)+(2*3)+(1*0)=76
76 % 10 = 6
So 5048-30-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-3-4-5-6-7-8-11-9(2)10/h3H,1,4-8H2,2H3
5048-30-6Relevant articles and documents
8-Endo cyclization of (alkoxycarbonyl)methyl radicals: Radical ways for preparation of eight-membered-ring lactones
Lee, Eun,Yoon, Cheol Hwan,Lee, Tae Hee,Kim, Sun Young,Ha, Tae Joon,Sung, Yong-Suk,Park, Sang-Hyun,Lee, Sangyoub
, p. 7469 - 7478 (2007/10/03)
Cyclization of (alkoxycarbonyl)methyl radicals generated from bromoacetates proceeds in the 8-endo made to generate heptanolactones. Three distinct types of 8-endo/5-exo tandem radical cyclizations produce different bicyclic heptanolactones. In certain cases, intramolecular free-radical attack on the heptanolactone carbonyl group initiates further skeletal rearrangement. Ab initio calculations indicate that the preference of the 8-endo cyclization over the 5-exo mode originates from the conformational bias of (alkoxycarbonyl)methyl radicals favoring the Z- over the E-conformation.
