| Weight | 183.254 g/mol |
|---|---|
| Formula | C13H13N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
N-Benzylaniline (103-32-2)
benzylaniline · N-phenylbenzylamine · benzylaniline thiocyanate
Score:
#1914 in Physics
,
#5991 in Chemistry
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- Simple direct titration of organolithium reagents using N-pivaloyl-o-toluidine and/or N-pivaloyl-o-benzylaniline (Journal of Organic Chemistry, 1989)
- Poly ( N Benzylaniline ) / ( Poly ( AMPS ) / WO 3 SolidState Electrochromic Cell (Journal of The Electrochemical Society, 1989)
- Intramolecular Interaction between Hydroxyl Group and -Eelctrons. V. Electronic Effect in Arylcarbinols and a Preliminary Note on the Interaction in Benzylaniline Derivatives (Bulletin of the Chemical Society of Japan, 1959)
- Synthesis and evaluation of a series of benzylaniline hydrochlorides as potential cytotoxic and antimitotic agents acting by inhibition of tubulin polymerization (Journal of Medicinal Chemistry, 1993)
- A UV-visible spectroelectrochemical study of the electropolymerisation of N-benzylaniline (Journal of Solid State Electrochemistry, 1999)
- Effect of tetramethylethlylenediamine on the metalation of N-methyl and N-phenylbenzylamine with n-butyllithium. Deuteration and electrophilic condensations of intermediate lithioamines. Cyclodehydrations to give N-substituted isoindolines (Journal of Organic Chemistry, 1971)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - benzylaniline
- N-phenylbenzylamine
- benzylaniline thiocyanate
- benzylaniline hydrochloride
- benzylaniline lithium salt
- benzylaniline potassium salt
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SMILESC1=CC=C(C=C1)CNC2=CC=CC=C2
-
InChIKeyGTWJETSWSUWSEJ-UHFFFAOYSA-N
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