35173-74-1

Basic information

• Product Name: 3,3'-bis-indolyl(phenyl)methane
• Synonyms: 3,3'-bis-indolyl(phenyl)methane
• CAS NO: 35173-74-1
• Molecular Weight: 322.409
• Mol File: 35173-74-1.mol
• Article Data: 189

Chemical Properties

• CAS DataBase Reference: 3,3'-bis-indolyl(phenyl)methane(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3'-bis-indolyl(phenyl)methane(35173-74-1)
• EPA Substance Registry System: 3,3'-bis-indolyl(phenyl)methane(35173-74-1)

Safety Data

• Hazardous Substances Data: 35173-74-1(Hazardous Substances Data)

Upstream product

• 120-72-9 indole 
• 20515-61-1 2-phenyl-4,4-dimethyloxazolidine 
• 17762-72-0 2-phenyl-tetrahydro-(2H)-1,3-oxazine 
• 31771-33-2 2-phenyl-4,4,6-trimethyltetrahydro-(2H)-1,3-oxazine 
• 100-52-7 benzaldehyde 
• 201024-81-9 C,N-diphenylnitrone 
• 13608-31-6 3,4,4-trimethyl-2-phenyl-1,3-oxazolidine 
• 538-51-2 benzylidene phenylamine 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 14850-89-6 (E)-N'-benzylidenebenzohydrazide 
• 5341-44-6 N-benzylidene-m-nitroaniline 
• 1613-89-4 (E)-N-benzylidene-4-chloroaniline 
• 51608-60-7 phenyl N-tosyl imine 
• 100-51-6 benzyl alcohol 

Downstream Products

• 1018685-92-1 6-(4-methoxyphenyl)-12-phenyl-5,7-dihydroindolo[2,3-b]carbazole 
• 29670-53-9 6,12-diphenyl-5,6,11,12-tetrahydroindolo[3,2-b]carbazole 
• 911303-02-1 3-[(4-methylphenylsulfonyl)(phenyl)methyl]-1H-indole 
• 27152-07-4 2,8-diphenyl-1,2,3,8-tetrahydroindolo[2,3-b]carbazole 
• 1529515-20-5 4-((1H-indol-3-yl)(phenyl)methyl)-N,N-dimethylaniline 
• 53924-36-0 4-((1H-indol-3-yl)(phenyl) methyl)-N,N-dimethylaniline 
• 120-72-9 indole 
• 910217-11-7 6,12-diphenyl-5,11-dihydroindolo[3,2-b]carbazole 

Relevant articles and documents

Lewis acid-catalyzed reactions in protic media. Lanthanide-catalyzed reactions of indoles with aldehydes or ketones

Lanthanide triflates were found to be effective catalysts for reactions of indoles with aldehydes or ketones in aqueous solution.

Highly enantioselective Friedel-Crafts reaction of indoles with imines by a chiral phosphoric acid

Highly enantioselective Friedel-Crafts reactions of indoles with imines catalyzed by a chiral phosphoric acid are developed, affording the 3-indolyl methanamine derivatives with up to >99% ee for a wide range of substrates. Copyright

Novel method for synthesis of unsymmetrical bis(indolyl)alkanes catalyzed by ceric ammonium nitrate (CAN) under ultrasonic irradiation

The reaction of indole with (1H-indol-3-yl)(alkyl) methanol was catalyzed efficiently by ceric ammonium nitrate under ultrasonic irradiation to afford the unsymmetrical bis(indolyl)alkane in good to excellent yields.

Solvent-free indoles addition to carbonyl compounds promoted by CeCl 3·7H2O-NaI-SiO2: An efficient method for the synthesis of streptindole

Efficient electrophilic substitution reactions of indoles with various carbonyl compounds proceed easily in solvent-free conditions using CeCl 3·7H2O-NaI-SiO2. system promoter, to afford the corresponding bis(1H-indol-3-yl

Preparation of G-CuO NPs and G-ZnO NPs with mallow leaves, investigation of their antibacterial behavior and synthesis of bis(indolyl)methane compounds under solvent-free microwave assisted dry milling conditions using G-CuO NPs as a catalyst

In this study, biogenic copper and zinc oxide nanoparticles (G-ZnONPs and G-CuONPs) were synthesized by the green synthesis method using Malva parviflora L. (Millow) leaf extract and the obtained nanoparticles were characterized in detail with UV-Vis, FTIR, SEM, XRD. The antibacterial properties of the synthesized nanoparticles on gram-positive and gram-negative bacteria were investigated and it was found that the nanoparticles had high antimicrobial activity in the results of the experiments. With the obtained G-CuONPs, the synthesis of bis(indolyl)methanes with the "green" one-pot synthesis using microwave was achieved quickly and with high efficiency, and the thermal behavior of the obtained products was investigated.

Application of alkaloid arundine and derivatives thereof in prevention and control of plant viruses and pathogenic bacteria

The invention relates to an application of alkaloid arundine and derivatives thereof in control of plant virus pathogens. It is found that arundine and derivatives I-1 to I-25 thereof show good anti-plant virus pathogen activity for the first time, and can well inhibit 14 plant germs including tobacco mosaic virus (TMV), cucumber fusarium wilt, peanut brown spot, apple ring spot, wheat sheath blight, corn bipolaris maydis, watermelon anthracnose, fusarium moniliforme, tomato early blight, wheat gibberellic disease, rice blast, phytophthora capsici, sclerotium of rape, cucumber gray mold and rice sheath blight.