5048-30-6 Usage
Uses
Used in Organic Synthesis:
7-Acetoxy-1-heptene is utilized as a key building block in the synthesis of a wide range of organic compounds. Its unique structure allows for the creation of various chemical entities, making it a valuable component in organic chemistry.
Used in Fragrance Industry:
In the fragrance industry, 7-Acetoxy-1-heptene is employed as a fragrance ingredient. Its fruity scent adds depth and complexity to perfumes and other personal care products, enhancing the overall sensory experience for consumers.
Used in Personal Care Products:
Beyond fragrances, 7-Acetoxy-1-heptene is also used in the formulation of various personal care products. Its incorporation contributes to the pleasant scent and overall appeal of these products, making them more attractive to users.
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 academic research and scientific papers
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.
New reagents for radical allylations
Curran,Yoo
, p. 6931 - 6934 (2007/10/02)
Three reagents are introduced for radical allylations: 3-phenylthio-2-bromopropene, 2,3-bis(trimethylstannyl)propene, and 3-tris(trimethylsilyl)silylthiopropene.
