504-96-1 Usage
Description
7,11,15-trimethyl-3-methylidene-hexadec-1-ene is a colorless liquid with the chemical formula C21H38. It is an organic compound characterized by its long hydrocarbon chain with three methyl groups at the 7th, 11th, and 15th carbon atoms, and a methylidene group at the 3rd carbon atom.
Uses
1. Enzyme Inhibition:
7,11,15-trimethyl-3-methylidene-hexadec-1-ene is used as an enzyme inhibitor due to its ability to interfere with the activity of certain enzymes, which can be beneficial in various applications.
2. Pharmaceutical Industry:
Used in the Pharmaceutical Industry, 7,11,15-trimethyl-3-methylidene-hexadec-1-ene serves as a key component in the development of drugs targeting specific enzymes. Its enzyme-inhibiting properties make it a valuable asset in the creation of therapeutic agents.
3. Chemical Synthesis:
In the field of chemical synthesis, 7,11,15-trimethyl-3-methylidene-hexadec-1-ene can be used as a starting material or an intermediate in the production of more complex organic compounds.
4. Industrial Solvent:
Due to its chemical properties, 7,11,15-trimethyl-3-methylidene-hexadec-1-ene can be employed as a solvent in various industrial processes, particularly where a non-polar, colorless liquid is required.
5. Research and Development:
7,11,15-trimethyl-3-methylidene-hexadec-1-ene is also used in research and development settings to study its interactions with different biological targets and to explore its potential applications in various fields, including medicine and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 504-96-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 504-96:
(5*5)+(4*0)+(3*4)+(2*9)+(1*6)=61
61 % 10 = 1
So 504-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H38/c1-7-18(4)12-9-14-20(6)16-10-15-19(5)13-8-11-17(2)3/h7,17,19-20H,1,4,8-16H2,2-3,5-6H3
504-96-1Relevant articles and documents
Development of synthetic routes to D,L-α-tocopherol (vitamin E) from biologically produced geranylgeraniol
Hyatt, John A.,Kottas, Gregg S.,Effler, Janet
, p. 782 - 787 (2013/09/06)
The use of the biologically derived diterpene alcohol geranylgeraniol was explored as an alternative to petrochemical-based isophytol as a side-chain synthon for producing D,L-α-tocopherol. Two routes were studied, both of which begin with allylic epoxidation followed by olefin hydrogenation to give epoxyphytol. Epoxyphytol can be reduced with Red-Al to provide phytan-1,3-diol which upon acid-catalyzed condensation with trimethylhydroquinone gives vitamin E in fair yield. In a higher-yielding process, epoxyphytol was deoxygenated with methylrhenium trioxide/triphenylphosphine to generate a mixture of phytol and isophytol (> 90% yield from geranylgeraniol). This mixture can serve as a "plug-in" replacement for isophytol in the final step of the currently practiced vitamin E chemistry. The use of methylrhenium trioxide to catalyse dehydration of vinyl dialkyl carbinols to 1,3-dienes was also demonstrated.
