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3-BENZYLOXYANILINE

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3-BENZYLOXYANILINE Basic information

Product Name:
3-BENZYLOXYANILINE
Synonyms:
  • Benzenamine, 3-(phenylmethoxy)-
  • M-(BENZYLOXY)ANILINE
  • 3-BENZYLOXYANILINE
  • AKOS BBB/398
  • AKOS BC-2549
  • TIMTEC-BB SBB000388
  • 3-Aminophenyl benzyl ether
  • 3-Benzyloxyaniline 98%
CAS:
1484-26-0
MF:
C13H13NO
MW:
199.25
EINECS:
216-056-6
Product Categories:
  • Anilines, Aromatic Amines and Nitro Compounds
  • Amines
  • C11 to C38
  • Nitrogen Compounds
Mol File:
1484-26-0.mol
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3-BENZYLOXYANILINE Chemical Properties

Melting point:
63-67 °C (lit.)
Boiling point:
170 °C(Press: 3 Torr)
Density 
1.129±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
pka
4.17±0.10(Predicted)
form 
Solid
color 
Pale brown
InChI
InChI=1S/C13H13NO/c14-12-7-4-8-13(9-12)15-10-11-5-2-1-3-6-11/h1-9H,10,14H2
InChIKey
IGPFOKFDBICQMC-UHFFFAOYSA-N
SMILES
C1(N)=CC=CC(OCC2=CC=CC=C2)=C1
CAS DataBase Reference
1484-26-0(CAS DataBase Reference)
EPA Substance Registry System
3-(Benzyloxy)aniline (1484-26-0)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
2811
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29222990

MSDS

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3-BENZYLOXYANILINE Usage And Synthesis

Chemical Properties

Beige to tan powder

Synthesis Reference(s)

Tetrahedron Letters, 23, p. 147, 1982 DOI: 10.1016/S0040-4039(00)86770-2

Synthesis

24318-00-1

1484-26-0

591-27-5

Using 1-(benzyloxy)-3-nitrobenzene as the starting material, the reaction was carried out using an experimental method similar to that of Example 59, in which ferrous acetate (II), nickel nitrate (II), or cobalt acetylacetonate (III) was chosen as the metal reducing agent. The experimental results are detailed in Table 11. The data of Examples 60 to 66 show that the reaction rate is significantly enhanced when metal compounds such as iron, nickel or cobalt salts and amine additives such as pyrrolidine are added to the catalytic reduction system of the present invention in the presence of a rhodium/carrier catalyst. Under this condition, functional groups such as benzyl ether, which are easy to reduce, are retained, and nitro is selectively reduced to amino, thereby increasing the yield of the target products 3-benzyloxyaniline and 3-aminophenol.

References

[1] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45
[2] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45
[3] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45
[4] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45
[5] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45

3-BENZYLOXYANILINE Preparation Products And Raw materials

Raw materials

3-BENZYLOXYANILINESupplier

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