51126-65-9

Basic information

• Product Name: potassium 1H-benzotriazolide
• Synonyms: potassium 1H-benzotriazolide;1H-Benzotriazole, potassium salt;1-Potassio-1H-benzotriazole
• CAS NO: 51126-65-9
• Molecular Formula: C₆H₄N₃*K
• Molecular Weight: 158.22
• EINECS: 256-999-0
• Mol File: 51126-65-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 276.1°C at 760 mmHg
• Flash Point: 133.9°C
• Appearance: /
• Vapor Pressure: 0.00491mmHg at 25°C
• CAS DataBase Reference: potassium 1H-benzotriazolide(CAS DataBase Reference)
• NIST Chemistry Reference: potassium 1H-benzotriazolide(51126-65-9)
• EPA Substance Registry System: potassium 1H-benzotriazolide(51126-65-9)

Safety Data

• Hazardous Substances Data: 51126-65-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C6H4N3.K/c1-2-4-6-5(3-1)7-9-8-6;/h1-4H;/q-1;+1

Upstream product

• 95-14-7 1,2,3-Benzotriazole 

Downstream Products

• 19759-89-8 4,4'-((1H-benzo[d][1,2,3]triazol-1-yl)-methylene)-bis(N,N-di-methylaniline) 
• 1362792-86-6 Br^(1-)*C₃₄H₃₈B₂N₃P₂⁽¹⁺⁾ 
• 69980-83-2 2-(2-aminoethyl)-1,2,3-benzotriazole 
• 209912-23-2 1-(2-phenylethynyl)-1H-1,2,3-benzotriazole 
• 209912-24-3 1-[2-(4-chlorophenyl)ethynyl]-1H-benzotriazole 
• 209912-21-0 1-[2-(4-methoxyphenyl)ethynyl]-1H-1,2,3-benzotriazole 
• 209912-22-1 1-[2-(4-methylphenyl)ethynyl]-1H-1,2,3-benzotriazole 
• 74731-95-6 2-(N-phthalimidoethyl)-1,2,3-benzotriazole 
• 26861-65-4 1-(2-aminoethyl)-1,2,3-benzotriazole 
• 16584-04-6 2-ethyl-2H-benzotriazole 
• 16584-05-7 1-ethylbenzotriazole 

Relevant articles and documents

Nucleophilic reactivities of the anions of nucleobases and their subunits

The kinetics of the reactions of different heterocyclic anions derived from imidazoles, purines, pyrimidines, and related compounds with benzhydrylium ions and structurally related quinone methides have been studied in DMSO and water. The second-order rate constants (logk2) correlated linearly with the electrophilicity parameters E of the electrophiles according to the correlation logk2 = sN(N+E) (H. Mayr, M. Patz, Angew. Chem. 1994, 106, 990-1010; Angew. Chem. Int. Ed. Engl. 1994, 33, 938-957) allowing us to determine the nucleophilicity parameters N and sN for these anions. In DMSO, the reactivities of these heterocyclic anions vary by more than six orders of magnitude and are comparable to carbanions, amide and imide anions, or amines. The azole anions are generally four to five orders of magnitude more reactive than their conjugate acids. Copyright