5413-09-2 Usage
Main Properties
1. Chemical Formula: C8H16O3
2. Carboxylic Acid: 3-Methoxyhexanoic acid is classified as a carboxylic acid due to the presence of a carboxyl group (-COOH) in its chemical structure.
3. Chain Length: It has a six-carbon chain, which contributes to its structure and reactivity.
4. Methoxy Group: A methoxy (-OCH3) group is attached to the third carbon of the chain.
5. Fruity Odor: It has a characteristic fruity smell, which makes it suitable for use in fragrances and flavorings.
6. Applications: 3-Methoxyhexanoic acid is widely used in the production of fragrances, flavorings, pharmaceuticals, food products, cosmetics, and as a precursor in the synthesis of various organic compounds.
7. Versatile: Due to its wide range of applications, it is considered a valuable chemical commodity in commercial and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 5413-09-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5413-09:
(6*5)+(5*4)+(4*1)+(3*3)+(2*0)+(1*9)=72
72 % 10 = 2
So 5413-09-2 is a valid CAS Registry Number.
5413-09-2Relevant articles and documents
Micromide and Guamamide: Cytotoxic Alkaloids from a Species of the Marine Cyanobacterium Symploca
Williams, Philip G.,Yoshida, Wesley Y.,Moore, Richard E.,Paul, Valerie J.
, p. 49 - 53 (2004)
Two new cytotoxins have been isolated from a species of marine cyanobacterium belonging to the genus Symploca that was collected in Guam. These new compounds, micromide (1) and guamamide (2), were accompanied by the known lipopeptides apramides A (3), B (4), and G (5). The planar structures of both alkaloids were elucidated by standard 2D NMR techniques, and the configurations of the amino acid-derived units in 1 were determined by chiral HPLC. The stereochemistry of the β-methoxyhexanoic acid in I was determined by derivatization with methyl D-mandelate, after acid hydrolysis, and comparison with synthetic standards.
