141-02-6 Usage
Description
DIOCTYL FUMARATE is a chemical compound with the chemical formula C22H38O4. It is an ester derived from di-n-octyl and fumaric acid. It has a density of 0.942 and a boiling point in the range of 211–220°C. However, no other chemical or physical data were found.
Uses
Used in Pharmaceutical Industry:
DIOCTYL FUMARATE is used as a pharmaceutical agent for its potential therapeutic applications. It is being investigated for its possible use in the treatment of various medical conditions due to its unique chemical properties.
Used in Chemical Industry:
DIOCTYL FUMARATE can be used as a raw material or intermediate in the synthesis of other chemicals and compounds. Its specific applications in the chemical industry may vary depending on the requirements of the end products being manufactured.
Please note that the provided materials do not give specific applications for DIOCTYL FUMARATE, so the uses listed above are general possibilities based on its chemical properties and potential industrial applications.
Flammability and Explosibility
Nonflammable
Safety Profile
Poison bp
intraperitoneal route. An eye and severe skin
irritant. Combustible when exposed to heat
or flame; can react with oxilzing materials.
To fight fire, use foam, CO2, dry chemical.
See also ESTERS and FUMARIC ACID
Check Digit Verification of cas no
The CAS Registry Mumber 141-02-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141-02:
(5*1)+(4*4)+(3*1)+(2*0)+(1*2)=26
26 % 10 = 6
So 141-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H36O4/c1-5-9-11-17(7-3)15-23-19(21)13-14-20(22)24-16-18(8-4)12-10-6-2/h13-14,17-18H,5-12,15-16H2,1-4H3/b14-13-/t17-,18-/m0/s1
141-02-6Relevant articles and documents
Chemistry in Water - Part VI. Catalytic Isomerization and Stereochemistry of Reduction of Acetylenics Mediated by Water-Soluble Phosphines
Larpent, Chantal,Meignan, Gerard
, p. 4331 - 4334 (2007/10/02)
Reaction of water-soluble phosphines with disubstituted electrodeficient alkynes in H2O (D2O) gives rise either to mixtures of cis and trans (dideuterated) olefins or specifically to trans (dideuterated) olefins, by simple control of the phosphine amount.A cis-trans olefin isomerization catalyzed by sulfonated phosphines occurs in water and allows the obtention of specifically trans disubstituted alkenes from the corresponding cis isomers.