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N,N'-Bis(phenyl)benzamidine

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Products Intro: Product Name:N,N′-Diphenylbenzamidine
CAS:2556-46-9
Purity:98% Remarks:B36492
Company Name: Energy Chemical  
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Products Intro: Product Name:N,N′-Diphenylbenzamidine
CAS:2556-46-9
Purity:purum, ≥98.0% (TLC) Package:1G-F;5G-F Remarks:NULL
Company Name: Baoji Didu Pharmaceutical and Chemical Co., Ltd  
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Products Intro: Product Name:N,N′-Diphenylbenzamidine
CAS:2556-46-9
Purity:98% Package:5g;10g
Company Name: Apollo Scientific Ltd.  
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Products Intro: CAS:2556-46-9
Remarks:OR11177
N,N'-Bis(phenyl)benzamidine Basic information
Product Name:N,N'-Bis(phenyl)benzamidine
Synonyms:N,N'-DIPHENYLBENZAMIDINE;TIMTEC-BB SBB008627;AURORA KA-4079;N,N'-Diphenylbenzenecarboxamidine;N1,N2-Diphenylbenzamidine;Benzenecarboximidamide, N,N'-diphenyl-;N,N'-Bis(phenyl)benzamidine
CAS:2556-46-9
MF:C19H16N2
MW:272.34
EINECS:219-872-0
Product Categories:Imines/Amidines;Nitrogen Compounds;Organic Building Blocks
Mol File:2556-46-9.mol
N,N'-Bis(phenyl)benzamidine Structure
N,N'-Bis(phenyl)benzamidine Chemical Properties
Melting point 125-129 °C
Boiling point 441.6±18.0 °C(Predicted)
density 1.03±0.1 g/cm3(Predicted)
pka7.70±0.10(Predicted)
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
10
HS Code 2921599090
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
N,N'-Bis(phenyl)benzamidine Usage And Synthesis
PreparationTo a three-necked, round-bottomed flask equipped with a mechanical stirrer, dropping funnel, and condenser is added 90.0 gm (0.46 mole) of pure dry benzanilide (see Note a) and 95 gm (0.46 mole) of phosphorus pentachloride (see Note b). The mixture is stirred to reduce the lumps and then heated for ½ hr at 110°C and 1½hr at 160°C, or until the evolution of hydrogen chloride ceases. Then 36.4 gm (0.46 mole) of KOH-dried pyridine (see Note c) is added with stirring, followed by 42.4 gm (0.46 mole) of freshly distilled aniline. The reaction mixture is heated at 160°C for about 20 min to discharge the red color, cooled to about 90°C, and 250 ml of water is added dropwise to precipitate the product in granular form. The product is filtered and added to 500 ml of 28% aqueous ammonia. The mixture is stirred while gently warming for 1 hr, filtered, dried, and recrystallized from 80% ethanol (8-10 ml/gm product) to afford 73-80% product, m.p. 144-145°C.
Preparation ofN,N'-Diphenylbenzamidine
N,N'-Bis(phenyl)benzamidine Preparation Products And Raw materials
Tag:N,N'-Bis(phenyl)benzamidine(2556-46-9) Related Product Information
N,N'-DIPHENYLBENZAMIDINE,N,N'-Diphenylbenzamidine, 98+% N,N'-Bis(phenyl)benzamidine N-HYDROXY-N,N'-DIPHENYL-BENSAMIDINE 4-[2-(Diisopropylamino)ethyl]-N,N'-diphenylbenzamidine N-Hydroxy-N,N'-diphenylbenzamidine 4(3H)-Quinazolinone, 3-(4-(4-oxo-2-(phenylimino)-3-thiazolidinyl)pheny l)-2-(4-((phenylmethylene)amino)phenyl)- AURORA KA-5452 AURORA KA-3169 AKOS 93542 ETHYL 4-[2-(4-METHOXYPHENYL)-4-OXOQUINAZOLIN-3(4H)-YL]BENZOATE AURORA KA-3364 AKOS AU36-M76 AKOS AU36-M78 AKOS AU36-M77 AURORA KA-4681 AURORA KA-3788 AURORA KA-4691 AURORA KA-5440