17951-14-3

Basic information

• Product Name: Guanidine, N,N,N',N'-tetramethyl-N''-(4-nitrophenyl)-
• CAS NO: 17951-14-3
• Molecular Formula: C11H16N4O2
• Molecular Weight: 236.274
• Mol File: 17951-14-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Guanidine, N,N,N',N'-tetramethyl-N''-(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Guanidine, N,N,N',N'-tetramethyl-N''-(4-nitrophenyl)-(17951-14-3)
• EPA Substance Registry System: Guanidine, N,N,N',N'-tetramethyl-N''-(4-nitrophenyl)-(17951-14-3)

Safety Data

• Hazardous Substances Data: 17951-14-3(Hazardous Substances Data)

Upstream product

• 56043-45-9 N,N,N',N'-tetramethylchlorformamidinium chloride 
• 100-01-6 4-nitro-aniline 
• 632-22-4 tetramethylurea 
• 2556-43-6 N,N,N',N'-tetramethyl-N-phenylguanidine 
• 2131-61-5 p-nitrophenyl isothiocyanate 

Downstream Products

• 1253284-59-1 C₁₄H₂₁N₄O₂⁽¹⁺⁾*Cl^(1-) 
• 25770-85-8 pyridine-2-azo-aniline 
• 136849-65-5 pyridine-2-azo-p-phenyltetramethylguanidine 

Relevant articles and documents

Redox-Active Guanidines with One or Two Guanidino Groups and Their Integration in Low-Dimensional Perovskite Structures

Redox-active guanidines are versatile reagents in redox and proton-coupled electron-transfer (PCET) reactions. Recently, they were integrated as sacrificial electron donors for the prohibition of metal oxidation in perovskite materials. Herein we report t

Synthesis of some of new substituted 2-(phenyl)-1,3-dimethyl- and -1,1,3,3-tetramethylguanidines

A series of new 2-(phenyl)-1,3- and 2-(phenyl)-1,3,3-tetramethylguanidines (a-k) were synthesized by reaction of different substituted aniline and urea derivatives in the presence of phosphorus oxychloride. The yields of products following extraction from

SYNTHESIS AND PROPERTIES OF PHENYL SUBTITUTED DERIVATIVES OF 2-PHENYL-1,1,3,3-TETRAMETHYLGUANIDINE

A series of 17 phenyl subtituted derivatives of 2-phenyl-1,1,3,3-tetramethylguanidine was synthesized.The structure and purity of these compounds were checked by means of elemental analyses, mass spectrometry, ultraviolet spectrophotometry, and 1H nuclear