Examples of 'epoxide group' in a sentence
Meaning of "epoxide group"
Epoxide group: Refers to a chemical group consisting of an oxygen atom bound to two adjacent carbon atoms. This phrase is commonly used in organic chemistry discussions and research
How to use "epoxide group" in a sentence
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epoxide group
Z is an epoxide group which may have a substituent.
A most preferred reactive end is an epoxide group.
The epoxide group is especially preferred.
Alkylene oxides contain an epoxide group.
The epoxide group is sometimes referred to as a glycidyl or oxirane group.
The nucleus has at least one reactive hydroxyl or epoxide group.
The epoxide group may be mentioned as an example of a hydroxyl group precursor.
The compound comprising at least one epoxide group may be a monoepoxide or a polyepoxide.
The epoxide group is also known as oxirane and glycidyl group.
The central nucleus is an epoxide compound with at least one reactive epoxide group.
The epoxide group can react with various curing agents.
It is noted that such adjacent hydroxyl groups may instead form an epoxide group.
The epoxide group appears to be an important substituent common to several angiogenesis inhibitors.
An ink can include a combination of such cationic reagents having at least one epoxide group.
Thereby especially the epoxide group as most toxic part of the molecule is degraded.
See also
The present invention also includes angiogenic inhibiting compounds that contain an epoxide group.
But altogether the epoxide group is crucial for the reactivity of the molecule.
The quinone carries a functional group capable of reacting with the epoxide group of the copolymer.
Typically, one epoxide group is required to interact with each phosphorous acid molecule.
Compound B can be prepared vía ring opening of a chiral or racemic epoxide group.
The latter monomers introduce an epoxide group into side chain of the PAC.
In some embodiments, the heterocyclic group is an epoxide group.
Prior to reaction, the epoxide group should be opened to provide the corresponding diol.
At least one R must have an epoxide group.
The epoxide group advantageously corresponds to the following formula I, where.
A reactive group I can be a terminal epoxide group for example.
An epoxide group of the formula,.
E may also be an acid-opened epoxide group.
The epoxide group can for example be present as a glycidyl group or a 3,4-epoxycyclohexyl group.
It possesses an indole-diterpene unit as well as a reactive epoxide group.
Compounds that contain more than one epoxide group ( that is, polyepoxides ) are preferred.
According to one particular embodiment, the R 2 group may comprise at least one epoxide group.
C60O may also be attached directly through an epoxide group on the fullerene to a stent.
During the process, however, this method presents side reaction of ring-opening of the epoxide group.
Epoxide group substitution was determined by methods known in the art to be 1.06 mmol / g.
Figure 3 displays the reaction of a polymer possessing an epoxide group with hexetidine.
Type C trichothecenes have an extra carbon 7, carbon 8 epoxide group.
The polyepoxides are those materials having a 1,2 epoxide group present in the molecule.
A compound as claimed by any one of Claims 1 to 8 wherein R1 and R2 form an epoxide group.
EXAMPLE 1 Synthesis of a molecule containing a reactive epoxide group and a pyrrolidyl group.
In a particular embodiment, Z is an epoxide group.
Reaction mixture is kept at 80°C until all of the epoxide group from GMA is reacted.
At least one epoxy resin having a functionality of greater than 0.8 epoxide group per molecule ;.
The polyepoxides which are phosphatized are those materials having a 1,2 epoxide group present in the molecule.
In a preferred embodiment, the organic R6 radical containing an epoxide group has 2 to 14 carbon atoms.
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