ChemicalBook--->CAS DataBase List--->6373-46-2

6373-46-2

6373-46-2 Structure

6373-46-2 Structure
IdentificationBack Directory
[Name]

4-BENZYLOXYANILINE
[CAS]

6373-46-2
[Synonyms]

AKOS B020052
AKOS BBB/085
ASISCHEM C15385
4-BENZLOXYANILINE
4-Benzyloxyanaline
4-BENZYLOXYANILINE
p-benzyloxy-anilin
p-Benzyloxyaniline
Lapatinib impurity D
Lapatinib Impurity 30
Aniline, p-(benzyloxy)-
4-Benzyloxyaniline ,97%
4-(phenylmethoxy)aniline
4-(benzyloxy)phenylamine
4-(benzyloxy)benzenamine
4-aminophenylbenzylether
4-Aminophenyl benzyl ether
Benzyl 4-aminophenyl ether
4-(phenylmethoxy)-benzenamin
4-(phenylmethoxy)benzenamine
Benzenamine, 4-(phenylmethoxy)-
[EINECS(EC#)]

228-917-3
[Molecular Formula]

C13H13NO
[MDL Number]

MFCD00025318
[MOL File]

6373-46-2.mol
[Molecular Weight]

199.25
Chemical PropertiesBack Directory
[Melting point ]

54-55 °C
[Boiling point ]

161-164 °C(Press: 0.25 Torr)
[density ]

1.129±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

powder to crystal
[pka]

5.17±0.10(Predicted)
[color ]

White to Gray to Brown
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29214200
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Sodium hydroxide-->Acetic acid-->Sodium sulfate-->Ammonium chloride-->Iron-->Benzyl bromide-->4-Nitrophenol-->Carbamic acid, N-[4-(phenylmethoxy)phenyl]-, 1,1-dimethylethyl ester-->AcetaMide, N-[4-(phenylMethoxy)phenyl]--->4-Benzyloxybromobenzene-->1-BENZYLOXY-4-NITROBENZENE-->4-Benzyloxyaniline hydrochloride-->Benzyl chloride-->4-Aminophenol
[Preparation Products]

5,8-Dihydro-5-imino-8-[[4-(phenylmethoxy)phenyl]imino]-1,4-naphthalenedione-->Benzamide, 2-amino-N-[4-(phenylmethoxy)phenyl]-
Hazard InformationBack Directory
[Uses]

4-Benzyloxyaniline is an intermediate in the synthesis of Acetaminophen-d3, the labeled analogue of Acetaminophen (A161220), an analgesic; antipyretic (1,2). It can be used to prepare N-(4-phenoxyphenyl)benzenesulfonamide derivatives that may be antagonists for the nonsteroidal progesterone receptor (3).
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