19759-89-8

Basic information

• Product Name: 4-[benzotriazol-1-yl-(4-dimethylaminophenyl)methyl]-N,N-dimethyl-anili ne
• Synonyms: 4-[benzotriazol-1-yl-(4-dimethylaminophenyl)methyl]-N,N-dimethyl-anili ne;1-[Bis[4-(dimethylamino)phenyl]methyl]-1H-benzotriazole
• CAS NO: 19759-89-8
• Molecular Formula: C₂₃H₂₅N₅
• Molecular Weight: 371.48
• Mol File: 19759-89-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 587.4°Cat760mmHg
• Flash Point: 309.1°C
• Appearance: /
• Density: 1.13g/cm³
• Vapor Pressure: 8.83E-14mmHg at 25°C
• Refractive Index: 1.625
• CAS DataBase Reference: 4-[benzotriazol-1-yl-(4-dimethylaminophenyl)methyl]-N,N-dimethyl-anili ne(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[benzotriazol-1-yl-(4-dimethylaminophenyl)methyl]-N,N-dimethyl-anili ne(19759-89-8)
• EPA Substance Registry System: 4-[benzotriazol-1-yl-(4-dimethylaminophenyl)methyl]-N,N-dimethyl-anili ne(19759-89-8)

Safety Data

• Hazardous Substances Data: 19759-89-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C23H25N5/c1-26(2)19-13-9-17(10-14-19)23(18-11-15-20(16-12-18)27(3)4)28-22-8-6-5-7-21(22)24-25-28/h5-16,23H,1-4H3

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 119-58-4 4,4'-bis(dimethylamino)benzhydrol 
• 1252931-45-5 Michler's Hydrol Blue 
• 51126-65-9 potassium salt of benzotriazole 

Downstream Products

• 95-14-7 1,2,3-Benzotriazole 
• 219653-95-9 1,1-di(4-dimethylaminophenyl)pentane 

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