Examples of 'nitrile group' in a sentence

Meaning of "nitrile group"

Nitrile group is a term used in chemistry to describe a functional group that contains a nitrogen atom bonded to two carbon atoms

How to use "nitrile group" in a sentence

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nitrile group
If another nitrile group is present it will also be hydrolyzed.
Furonitrile is a colorless derivative of furan possessing a nitrile group.
The molecule features a nitrile group attached to an amino group.
The method utilizes a decoy agent containing a nitrile group.
The nitrile group is tethered to the aromatic ring by a removable linker.
When ethanol is employed the nitrile group is converted to a COOEt group.
The nitrile group is converted into tetrazole by reaction with tributyltin azide.
Nitrile anions are nitriles lacking a proton at the position α to the nitrile group.
Cyclopropyl cyanide is an organic compound consisting of a nitrile group as a substituent on a cyclopropane ring.
The nitrile group is then reduced to furnish the aldehyde XII.
This method also hydrogenates not only a nitrile group but also an unsaturated groups.
Acrylic shows low UPF due to the dipole interactions of the nitrile group.
THC derivatives that have a terminal nitrile group can be prepared from halides or sulfonate esters.
A nitrile group is a group CN.
The electron withdrawing effect of the trichloromethyl group activates the nitrile group for nucleophilic additions.

See also

Represents a nitrile group or an amino group optionally substituted with,.
However, none of the known examples contain a nitrile group.
Note that partial hydrolysis of the nitrile group occurs under the Suzuki reaction conditions.
A nitrile group may be hydrolysed to give an amide, acid or ester.
Finally acidic hydrolysis of the nitrile group gives the desired acids H.
A nitrile group can be hydrolyzed, reduced, or ejected from a molecule as a cyanide ion.
Hydrolysis of the nitrile group using aq . conc.
In the present invention, cyano group is used synonymously with nitrile group.
Product analogue where the nitrile group has been hydrolysed to an amide,.
The nitrile group is transformed to an amidino group using a modified thio-Pinner sequence.
By reducing the pH value, a saponification of the nitrile group takes place.
In aliphatic nitriles, the nitrile group may be attached to a primary or secondary carbon.
A process according to claim 8, wherein the monomer having a nitrile group is acrylonitrile.
However, preferably a nitrile group is transformed into a corresponding tetrazole before hydrolysis of an ester.
Process ( d ) is carried out according to known methods for the introduction of a nitrile group.
Thus the desired intermediate 12 having a nitrile group and a free amino group is obtained.
As a bifunctional compound, trichloroacetonitrile can react at both the trichloromethyl and the nitrile group.
The alkylating agent may, alternatively, contain a nitrile group which is reduced to form an amine.
The hydrolysis / decarboxylation reaction condition also causes the hydrolysis of the nitrile group.
The highly electron-withdrawing effect of this nitrile group renders this hydrogen markedly more acidic.
In another embodiment, the carbonyl compound contains a reactive carbonyl group and a reactive nitrile group.
A nitrile group at the R ¹ position can be reduced to carboxaldehyde and hydroxymethyl groups.
The term " cyanoamino " used herein refers to nitrogen radical with nitrile group attached thereto.
The nitrile group is hydrolized to give L-carnitine chloride which is finally converted to L-carnitine.
By mononitrile compound is meant an organic compound including a single nitrile group of formula - CN.
The nitrile group can be converted to an amide 30 eq.
In step 4 of the process, the R group on the nitrogen is replaced with a nitrile group.
Equation 1 of Scheme 9 depicts the hydrolysis of a nitrile group to the corresponding carboxylic acid.
The nitrile group is subsequently reduced to give amine 10c.
In a preferred embodiment of the invention R1 is a nitrile group.
The nitrile group thus functions as a “ masked ” acid group.
A stilbene derivative or salt of claim 1, wherein X is a nitrile group.
The nitrile group of the resulting ether ( 9 ) is then hydrolyzed to form the primary amide.
In the formulae, R6 represents an ester or nitrile group and L ' represents a leaving group.
Further in the formula ( I ), Y represents a hydrogen atom, a nitro group or a nitrile group.

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