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Merck
모든 사진(1)

Key Documents

189049

Sigma-Aldrich

2-Benzyloxyaniline

97%

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About This Item

Linear Formula:
C6H5CH2OC6H4NH2
CAS Number:
Molecular Weight:
199.25
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

97%

mp

35-39 °C (lit.)

SMILES string

Nc1ccccc1OCc2ccccc2

InChI

1S/C13H13NO/c14-12-8-4-5-9-13(12)15-10-11-6-2-1-3-7-11/h1-9H,10,14H2

InChI key

PLPVLSBYYOWFKM-UHFFFAOYSA-N

일반 설명

2-Benzyloxyaniline is an important intermediate in organic synthesis.

애플리케이션

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.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

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)
Selective alkylation of aminophenols.
Wang R and Xu J.
ARKIVOC (Gainesville, FL, United States), 293-299 (2010)
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
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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