Examples of 'carbamic' in a sentence
Meaning of "carbamic"
Carbamic (adjective): Relating to carbamic acid or its derivatives. In chemistry, carbamic acid is a compound with the formula NH2COOH. Carbamic compounds often involve the attachment of a carbamate group (-NH(C=O)OR) to a molecule
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- Of or pertaining to carbamic acid or its derivatives.
How to use "carbamic" in a sentence
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carbamic
A number of carbamic acid compounds have been described.
Carbamates usually refer to esters of carbamic acid.
Ester of carbamic acid useful as a microbicide and preservative.
Methyl carbamate is the simplest ester of carbamic acid.
Carbamic acid is a planar molecule.
Production of unsaturated carbamic acid derivative.
Carbamic acid derivatives and method for preparing the same.
The main metabolite is the glucuronidated tocainide carbamic acid.
Preferred substituents for carbamic and carbonic acids are alkyl and phenyl.
A carbamate is an ester of carbamic acid.
Carbamic acid compounds comprising an amide linkage for the treatment of malaria.
In this case the reaction is believed to proceed vía carbamic acid.
A step of separating the precipitated carbamic acid derivative of arbekacin including arbekacin carbonate.
A known method can be used to produce these carbamic acid esters.
A novel ester of carbamic acid useful in controlling the growth and proliferation of microorganisms.
See also
Derivatives of carbamic acid.
Carbamic acid ester derivatives for the production of isocyanate and aromatic hydroxy compounds.
The reaction of moisture with residual isocyanate forms carbamic acid.
Unlike carbamic acids, the esters are stable.
Structurally, it is an ester of carbamic acid.
Furthermore, the carbamic group is essential for activity.
A water soluble ammonium polyphosphate ; and a carbamic acid derivative.
Carbamic acid derivatives, their production and use.
In order to obtain respectively the activated carbamic acid derivatives containing formulae,.
The carbamic acid derivative may be guanidine or dicyandiamide, but is preferably urea.
There are many known ways of preparing amides, urea carbamic esters or sulfonamids.
Carbamic acids are unstable, but the salts of these elusive acids are well known.
This preparation may be done, for example by halogenating the carboxylic or carbamic acid.
The carbamic acid ester can be transformed to the free amine as shown in scheme 2.
Acyl is derived from an organic carboxylic acid, carbonic acid or carbamic acid.
Typical examples of reactive derivatives are carboxylic, carbamic or sulfamic acid halides, preferably chlorides.
Two reaction products are localised, the ammonium carbamate and the carbamic acid.
The present invention relates to carbamic acid derivatives, and their production and use.
A carbamic acid moiety activated with a leaving group, for example a carbamyl chloride moiety ;.
The isocyanate adds water in a nucleophilic addition step to yield a carbamic acid ( aka urethane ).
Examples of the carbamic acid blocker include N-phenylcarbamate phenyl.
Where the allyl group is part of carbamate, deallylation affords the corresponding carbamic acid.
The N-substituted carbamic acid ester can be used as a precursor of isocyanate.
The organoborane-amine dissociates in the coating composition vía in-situ formation of the carbamic zwitterion.
Oxazolines, oxazolidinones and derivatives of carbamic acid are compounds inhibiting the migration of Langerhans cells.
Typically, the optional and / or free amine promotes the reaction that forms the carbamic zwitterion.
Carbamic acid, ammonium salt.
A carbamate is an organic compound derived from carbamic acid NH2COOH.
Step ( c ), a step of producing the carbamic acid ester by reacting the hydroxy composition c and urea.
Treatment of the - NCO isocyanate in order to obtain said stable carbamic acid derivative.
Carbamates are esters of carbamic acid, NH2COOH, an unstable compound.
The carbonic acid derivative is a carbonic acid ester, an N-unsubstituted carbamic acid ester or urea.
Carbamic acid is the compound with the formula H2NCO2H.
The terminology " in-situ " refers to forming the carbamic zwitterion in the coating composition.
Examples of compounds represented by formula ( 41 ) above may include urea compounds and carbamic acid esters.
