55348-86-2 Usage
Chemical structure
A long-chain unsaturated fatty acid with a carboxyl group and a formyl group.
Natural occurrence
Found in certain bacteria.
Biosynthesis
Acts as an intermediate in the biosynthesis of linoleic acid, an essential polyunsaturated fatty acid.
Metabolic pathways
Involved in important metabolic pathways.
Potential roles
Studied for its potential role in inflammation, oxidative stress, and lipid metabolism.
Biomarker
Identified as an important biomarker for certain bacteria.
Applications
Has potential applications in the development of antimicrobial agents and dietary supplements.
Research status
Further research is needed to fully understand the biological functions and potential practical applications of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 55348-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,4 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55348-86:
(7*5)+(6*5)+(5*3)+(4*4)+(3*8)+(2*8)+(1*6)=142
142 % 10 = 2
So 55348-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O3/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15/h3-6,11H,1-2,7-10H2,(H,14,15)/b5-3+,6-4+
55348-86-2Relevant academic research and scientific papers
ACYCLIC ALKENES VIA OZONOLYSIS OF MULTI-UNSATURATED CYCLOALKENES
-
Paragraph 00117-00118, (2015/02/02)
A method of making a compound of formula (IIa) by selective ozonolysis of a compound of formula (I) is provided, wherein A is a C6-C10 alkene chain with at least one double bond, R1 is a C1-C10 alkyl, and R3 is an oxygen-containing functional group.
OZONOLYSIS OF ALKENES AND THE REACTIONS OF POLYFUNCTIONAL COMPOUNDS XL. SYNTHESIS OF (Z,Z)-, (E,E)-, AND (E/Z,Z/E)-7,11-HEXADECADIEN-1-YL ACETATES - COMPONENTS OF THE SEX PHEROMONE OF PECTINOPHORA GOSSYPIELLA (SAUNDERS)
Odinokov, V. N.,Mukhametzyanova, R. S.,Galeeva, R. I.,Ishmuratov, G. Yu.,Tolstikov, G. A.
, p. 1399 - 1407 (2007/10/02)
A new approach is proposed for the synthesis of (Z,Z)-, (E,E)-, and (E/Z,Z/E)-7,11-hexadecadien-1-yl acetates, which are components of the sex pheromone of the pink bollworm (Pectinophora Gossypiella).The method is based on the selective ozonolysis of (Z,Z,Z)-, (E,E,E), and (E,E,Z)-cyclododecatrienes.
