189049
2-Benzyloxyaniline
97%
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About This Item
Linear Formula:
C6H5CH2OC6H4NH2
CAS Number:
Molecular Weight:
199.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
InChI
1S/C13H13NO/c14-12-8-4-5-9-13(12)15-10-11-6-2-1-3-7-11/h1-9H,10,14H2
SMILES string
Nc1ccccc1OCc2ccccc2
InChI key
PLPVLSBYYOWFKM-UHFFFAOYSA-N
assay
97%
mp
35-39 °C (lit.)
General description
2-Benzyloxyaniline is an important intermediate in organic synthesis.
Application
2-Benzyloxyaniline was used to investigate crystal structure of benzyloxybenzoic acids and benzyloxyanilines by X-ray powder diffraction technique. It was also used in the synthesis of 2-benzyloxyphenylhydrazine.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Structural study of four benzyloxybenzoic acids and benzyloxyanilines using X-ray powder diffraction: interplay of strong and weak intermolecular interactions.
Chattopadhyay B, et al.
CrystEngComm, 15(6), 1077-1085 (2013)
Catherine Roullier et al.
Bioorganic & medicinal chemistry letters, 20(15), 4582-4586 (2010-06-24)
A new aryl-hydrazide l-glutamic acid derivative, pygmeine (3), was isolated from a methanolic extract of Lichina pygmaea, a marine lichen. Synthetic derivatives obtained via a two-step coupling of l-glutamic acid with phenylhydrazine moieties were useful to elucidate the structure of
Selective alkylation of aminophenols.
Wang R and Xu J.
ARKIVOC (Gainesville, FL, United States), 293-299 (2010)
H Ottosson et al.
Scientific reports, 6, 36692-36692 (2016-11-09)
A new concept for treatment of infections is induction of our own antimicrobial peptides and the presented novel class of inducer, aroylated phenylenediamines (APDs), gives up to 20 to 30-fold induction of the human antimicrobial peptide LL-37, in vitro. In
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