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N,N,N′,N′-Tetramethylformamidinium chloride

N,N,N′,N′-Tetramethylformamidinium chloride is the simplest representative of quaternary formamidinium cations of the general formula + with a chloride as a counterion in which all hydrogen atoms of the protonated formamidine + are replaced by methyl groups.

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Overview

Preparation

Properties

Applications

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Map overview Semantic statistics

N,N,N′,N′-Tetramethylformamidinium chloride

Nodes50
Edges49
Triples20
Avg. degree1.96
Density0.04
Components1

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N,N,N′,N′-Tetramethylformamidinium chloride

Top relations

has application · 6
N,N,N′,N′-Tetramethylformamidinium chloride → CH, CH-acidic, For, NR1R2, Tetramethylformamidinium, The
related to Preparation · 5
N,N,N′,N′-Tetramethylformamidinium chloride → Bredereck's, CH3, DMF, It, Tetramethylformamidinium
related to Properties · 3
N,N,N′,N′-Tetramethylformamidinium chloride → After, For, Tetramethylformamidinium
is a · 1
N,N,N′,N′-Tetramethylformamidinium chloride → simplest representative of quaternary formamidinium cations of the general formula

Important terminology Word statistics

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Important terminology

-tetramethylformamidinium chloride dimethylamino sodium bis salt solid formamidinium r2n nr2 dimethylformamide aminomethylenation formula also counterion hydrogen basic carbene references reagent

Entity relationships Subject–Predicate–Object triples

SubjectPredicateObjectConfidenceSrc
N,N,N′,N′-Tetramethylformamidinium chlorideis asimplest representative of quaternary formamidinium cations of the general formula0.90text
indolesinstance ofcyanoacetate in practically quantitative yields.The aminomethylenation provides intermediates for the synthesis of heterocycles0.80text
pyrimidinesinstance ofcyanoacetate in practically quantitative yields.The aminomethylenation provides intermediates for the synthesis of heterocycles0.80text
pyridinesinstance ofcyanoacetate in practically quantitative yields.The aminomethylenation provides intermediates for the synthesis of heterocycles0.80text
quinolones.Ninstance ofcyanoacetate in practically quantitative yields.The aminomethylenation provides intermediates for the synthesis of heterocycles0.80text
Ninstance ofcyanoacetate in practically quantitative yields.The aminomethylenation provides intermediates for the synthesis of heterocycles0.80text
N,N,N′,N′-Tetramethylformamidinium chloridehas applicationTetramethylformamidinium0.60section
N,N,N′,N′-Tetramethylformamidinium chloridehas applicationCH0.60section
N,N,N′,N′-Tetramethylformamidinium chloridehas applicationNR1R20.60section
N,N,N′,N′-Tetramethylformamidinium chloridehas applicationCH-acidic0.60section
N,N,N′,N′-Tetramethylformamidinium chloridehas applicationFor0.60section
N,N,N′,N′-Tetramethylformamidinium chloridehas applicationThe0.60section

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