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4-Benzyloxyaniline hydrochloride

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4-Benzyloxyaniline hydrochloride Basic information

Product Name:
4-Benzyloxyaniline hydrochloride
Synonyms:
  • P-BENZYLOXYANILINE HYDROCHLORIDE
  • TIMTEC-BB SBB000742
  • 4-BENZYLOXY ANILINE HCL
  • 4-BENZYLOXYANILINE HYDROCHLORIDE
  • 4-BENZYLOXYANILINIUM CHLORIDE
  • 4-AMINOPHENYL BENZYL ETHER HYDROCHLORIDE
  • 4-Aminodiphenyletherhydrochloride
  • 4-BenzyloxyAnilideHydrochloride
CAS:
51388-20-6
MF:
C13H14ClNO
MW:
235.71
EINECS:
257-170-6
Product Categories:
  • Amine Salts
  • Building Blocks
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • Anilines, Aromatic Amines and Nitro Compounds
Mol File:
51388-20-6.mol
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4-Benzyloxyaniline hydrochloride Chemical Properties

Melting point:
228 °C (dec.)(lit.)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Slightly soluble in water insoluble in ether sparingly soluble in methanol
form 
Crystalline Powder
color 
Brownish
BRN 
3633307
InChI
InChI=1S/C13H13NO.ClH/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11;/h1-9H,10,14H2;1H
InChIKey
KQBDLOVXZHOAJI-UHFFFAOYSA-N
SMILES
C1(=CC=C(N)C=C1)OCC1=CC=CC=C1.Cl
CAS DataBase Reference
51388-20-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-36/37
WGK Germany 
3
RTECS 
BW7615000
Hazard Note 
Irritant
HS Code 
29222900

MSDS

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4-Benzyloxyaniline hydrochloride Usage And Synthesis

Chemical Properties

BROWNISH CRYSTALLINE POWDER

Uses

4-(benzyloxy)aniline hydrochloride can be used in chemical synthesis studies.

Synthesis

100-02-7

100-39-0

51388-20-6

(11-1) Synthesis of 4-benzyloxyaniline hydrochloride: 4.17 g of 4-nitrophenol was dissolved in 40 mL of ethanol, 2.5 g of potassium carbonate and 3.9 mL of benzyl bromide were added to the solution, and the mixture was heated and refluxed for 1.5 hours. After completion of the reaction, the reaction mixture was cooled, the precipitated crystals were collected by filtration and washed with deionized water. Subsequently, the resulting crude product was recrystallized from ethanol to give 6.4 g (94% yield) of colorless needle-like 4-nitrophenol benzyl ether.

References

[1] Patent: US5166403, 1992, A

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