ChemicalBook > Product Catalog > Organic Chemistry > Amides > Acyclic polyamines and their derivatives > 4-Benzyloxyaniline hydrochloride
4-Benzyloxyaniline hydrochloride
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
- Language:English Provider:4-Aminophenyl benzyl ether hydrochloride
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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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
4-Benzyloxyaniline hydrochlorideSupplier
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