2380-27-0 Usage
Description
METHYL 12-OXOOCTADECANOATE, also known as a long chain keto fatty acid, is a light brown solid that has been studied for its reaction with hydrazoic acid. It is characterized by its unique chemical properties and potential applications in various industries.
Uses
1. Used in Pharmaceutical Industry:
METHYL 12-OXOOCTADECANOATE is used as a chemical intermediate for the preparation of various pharmaceutical compounds. Its application is due to its ability to react with other chemicals, such as thiocarbohydrazide, to form derivatives with potential therapeutic properties.
2. Used in Chemical Synthesis:
METHYL 12-OXOOCTADECANOATE serves as a key component in the synthesis of complex organic molecules. Its application is attributed to its reactivity and the formation of valuable products, such as methyl hexahydro-3-hexyl-6-thioxo-1,2,4,5-tetrazine-3-undecanoate, which is a hexahydrothioxotetrazine fatty derivative.
Check Digit Verification of cas no
The CAS Registry Mumber 2380-27-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2380-27:
(6*2)+(5*3)+(4*8)+(3*0)+(2*2)+(1*7)=70
70 % 10 = 0
So 2380-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H36O3/c1-3-4-5-12-15-18(20)16-13-10-8-6-7-9-11-14-17-19(21)22-2/h3-17H2,1-2H3
2380-27-0Relevant articles and documents
Synthesis, Characterisation, and Transformations of a Lipid Cyclic Peroxide
Bascetta, Emanuele,Gunstone, Frank D.,Scrimgeour, Charles M. S.
, p. 2199 - 2206 (2007/10/02)
Photosensitised oxidation of (9E,11E)-methyl octadeca-9,11-dienoate gave an unsaturated cyclic peroxide (epidioxide) in high yield.This was characterised spectroscopically.The peroxide underwent facile rearrangement to a furanoid ester under a variety of reaction conditions.Catalytic reduction of the unsaturated peroxide cleaved the O-O bond.Bromination and epoxidation gave dibromo and epoxy esters respectively with the peroxide group still intact.
