1115-94-2 Usage
Type of fatty acid
Branched-chain saturated fatty acid It has a main carbon chain of 11 carbon atoms with three additional methyl groups attached, making it branched and saturated (no double bonds between carbon atoms).
Methyl group positions
2nd, 6th, and 10th carbon atoms The three methyl groups are attached to these specific carbon atoms, giving the compound its unique structure and properties.
Natural occurrence
Commonly found in nature 2,6,10-trimethylundecanoic acid is a component of many natural fats and oils, making it a naturally occurring compound.
Industrial applications
Production of various chemical compounds It is often used in the production of esters, which are widely used in the fragrance and flavor industries.
Use in pharmaceuticals and cosmetics
Synthesis and formulation 2,6,10-trimethylundecanoic acid is utilized in the synthesis of pharmaceuticals and cosmetics, making it an important compound in these industries.
Unique properties and applications
Versatile compound Due to its unique structure and properties, 2,6,10-trimethylundecanoic acid is an important and versatile compound used in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1115-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1115-94:
(6*1)+(5*1)+(4*1)+(3*5)+(2*9)+(1*4)=52
52 % 10 = 2
So 1115-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H28O2/c1-11(2)7-5-8-12(3)9-6-10-13(4)14(15)16/h11-13H,5-10H2,1-4H3,(H,15,16)
1115-94-2Relevant articles and documents
THE IDENTIFICATION OF 2,3-DIMETHYL-5-(2,6,10-TRIMETHYLUNDECYL)THIOPHENE, A NOVEL SULPHUR CONTAINING BIOLOGICAL MARKER
Damste, J.S.Sinninghe,Kock-van Dalen, A.C.,de Leeuw, J.W.,Schenck, P.A.
, p. 957 - 960 (1987)
The identification of 2,3-dimethyl-5-(2,6,10-trimethylundecyl)thiophene as a major constituent of certain petroleums and sediment extracts was confirmed by synthesis of the standard.
