6322-39-0 Usage
Uses
Used in Rubber and Petroleum Industry:
1,2-bis(4-nitrophenyl)guanidine is used as an antioxidant and stabilizer for preventing oxidation and deterioration of rubber and petroleum products.
Used in Dye Production:
1,2-bis(4-nitrophenyl)guanidine is used as a reagent in the production of dyes.
Used in Pharmaceutical Industry:
1,2-bis(4-nitrophenyl)guanidine is used as a reagent in the synthesis of various pharmaceutical compounds.
Used in Organic Compound Synthesis:
1,2-bis(4-nitrophenyl)guanidine is used as a reagent in the synthesis of various organic compounds.
Note: While 1,2-bis(4-nitrophenyl)guanidine has various applications, it has been identified as a potential skin irritant and may have harmful effects on aquatic organisms. Therefore, proper precautions should be taken when handling and disposing of 1,2-bis(4-nitrophenyl)guanidine.
Check Digit Verification of cas no
The CAS Registry Mumber 6322-39-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6322-39:
(6*6)+(5*3)+(4*2)+(3*2)+(2*3)+(1*9)=80
80 % 10 = 0
So 6322-39-0 is a valid CAS Registry Number.
6322-39-0Relevant academic research and scientific papers
Copper-catalyzed guanidinylation of aryl iodides: The formation of N,N′-disubstituted guanidines
Cortes-Salva, Michelle,Nguyen, Be-Lan,Cuevas, Javier,Pennypacker, Keith R.,Antilla, Jon C.
supporting information; experimental part, p. 1316 - 1319 (2010/06/15)
Chemical Equation Presented A copper-catalyzed cross-coupling reaction of guanidine nitrate with aryl iodides was used for the formation of N,N′-disubstituted guanidines to be used as potential therapeutics for strokes. A relatively inexpensive commercially available guanidine salt and a series of aryl iodides together with copper iodide and N,N-diethylsalicylamide as an efficient catalyst/1 igand system provided a simple diarylation procedure.
Synthetic routes to N-Pmc-N′,N″-disubstituted guanidines via EDCI-mediated guanylation of amines with N-Pmc-N′-substituted thioureas
Flemer Jr., Stevenson,Madalengoitia, Jose S.
, p. 1848 - 1860 (2008/02/10)
An overview of the facile and high-yielding EDCI-mediated reaction of amines with N-Pmc-N′-alkyl thioureas to afford guanidines is presented, in which the general scope and limitations of the reaction are probed. It was found that the N-sulfonyl-N′-substi
