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Amidine

Amidines are organic compounds with the functional group RC(NR)NR2, where the R groups can be the same or different. They are the imine derivatives of amides (RC(O)NR2). The simplest amidine is formamidine, HC(=NH)NH2.

Applications, Preparation & Nomenclature

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Overview

Preparation

Acid-base chemistry

Applications

Nomenclature

Derivatives

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Map overview Semantic statistics

Amidine

Nodes58
Edges57
Triples35
Avg. degree1.97
Density0.034483
Components1

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Amidine

Top relations

related to Nomenclature · 10
Amidine → Carboxamidines, Formally, IUPAC, NH2, NR, NR2, OH, RnE, The, When
related to Preparation · 8
Amidine → Bronsted, Catalysis, Instead, Lewis, Likewise, Pinner, Reaction, Treatment
related to Acid-base chemistry · 5
Amidine → Amidines, C-N, Protonation, The, This
has application · 4
Amidine → Examples, FA, Formamidinium, Several
see also · 2
Amidine → Guanidines, Imidazolines
is a · 1
Amidine → carboxamidine or carboximidamide

Important terminology Word statistics

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Important terminology

amidines nr nr2 amides formamidinium cations group rc derivatives reaction acid resulting nitrogen organic compounds nh2 examples include chemistry amidinate

Entity relationships Subject–Predicate–Object triples

SubjectPredicateObjectConfidenceSrc
Amidineis acarboxamidine or carboximidamide0.90text
aluminium trichloride promote the direct amination of nitrilesinstance ofLewis acids0.80text
orinstance ofLewis acids0.80text
in certain exceptional casesinstance ofLewis acids0.80text
of amides.Catalysis is not required for direct amination of an imidoyl chlorideinstance ofLewis acids0.80text
methyl lithiuminstance ofand can be accessed by reaction of a carbodiimide with an organometallic compound0.80text
Amidinehas applicationSeveral0.60section
Amidinehas applicationExamples0.60section
Amidinehas applicationFormamidinium0.60section
Amidinehas applicationFA0.60section
Amidinerelated to Acid-base chemistryAmidines0.60section
Amidinerelated to Acid-base chemistryProtonation0.60section

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