CAS 141-02-6
:Fumarate de 2-éthylhexyle
- 2-Butenedioic acid (2E)-, 1,4-bis(2-ethylhexyl) ester
- 2-Butenedioic acid (2E)-, bis(2-ethylhexyl) ester
- 2-Butenedioic acid (E)-, bis(2-ethylhexyl) ester
- 2-Ethylhexyl fumarate
- Bis(2-ethylhexyl) fumarate
- DOF
- Dioctyl fumarate
- Dioctylfumarate
- Fumaric acid, bis(2-ethylhexyl) ester
- Maximol FOK 670
- RC Comonomer DOF
- bis(2-ethylhexyl) (2E)-but-2-enedioate
- bis[(2S)-2-ethylhexyl] (2Z)-but-2-enedioate
- Voir plus de synonymes
Bis(2-ethylhexyl) Fumarate
CAS :Formule :C20H36O4Degré de pureté :>98.0%(GC)Couleur et forme :Colorless to Almost colorless clear liquidMasse moléculaire :340.50Bis(2-Ethylhexyl) Fumarate
CAS :Bis(2-Ethylhexyl) FumarateDegré de pureté :98%Masse moléculaire :340.5g/molBis(2-ethylhexyl) Fumarate
CAS :Produit contrôléApplications BIS(2-ETHYLHEXYL) FUMARATE (cas# 141-02-6) is a useful research chemical.
Formule :C20H36O4Couleur et forme :NeatMasse moléculaire :340.5Bis(2-ethylhexyl) fumarate
CAS :Bis(2-ethylhexyl) fumarate is a synthetic chemical compound that has been used in the synthesis of clostridium botulinum. It is a white solid with a constant melting point. This compound can be synthesized via the reaction of propiolic acid and maleic anhydride, which produces a carbon-carbon bond. Bis(2-ethylhexyl) fumarate is not estrogenic, but it does bind to the human estrogen receptor. The binding affinity for this receptor has been shown to be lower than other compounds such as diethylstilbestrol and ethinyl estradiol. Bis(2-ethylhexyl) fumarate also reacts with polyvinyl chloride and crotonic acid, forming crosslinked polymers that are photoreactive.
Formule :C20H36O4Degré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :340.5 g/mol





