4-BENZYLOXYANILINE

  • Name:4-BENZYLOXYANILINE
  • CAS:6373-46-2
  • Purity:99%
Inquiry

Details

Quality products?make an important contribution to long-term revenue and profitability. Manufacturer Sells Best Quality 4-BENZYLOXYANILINE 6373-46-2 with stock

1.What is the 4-BENZYLOXYANILINE ?

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).

benzyl 4-nitrophenyl ether
1145-76-2

benzyl 4-nitrophenyl ether

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

p-benzyloxyaniline
6373-46-2

p-benzyloxyaniline

4-amino-phenol
123-30-8

4-amino-phenol

Conditions
Conditions Yield
With potassium fluoride; polymethylhydrosiloxane; palladium diacetate; In tetrahydrofuran; at 20 ℃; for 0.5h;
56%
14%
28%
benzyl 4-nitrophenyl ether
1145-76-2

benzyl 4-nitrophenyl ether

p-benzyloxyaniline
6373-46-2

p-benzyloxyaniline

Conditions
Conditions Yield
With hydrazine hydrate; In methanol; at 26 ℃; for 0.25h; Reagent/catalyst; Solvent;
100%
With hydrogen; In ethyl acetate; at 20 ℃; for 4h; under 7600.51 Torr; chemoselective reaction;
99%
With Fe3O4Rh; hydrazine hydrate; In ethanol; at 80 ℃; for 10h; Inert atmosphere;
99%
With 1,1,3,3-Tetramethyldisiloxane; In ethanol; ethyl acetate; at 20 ℃; for 4h; chemoselective reaction; Inert atmosphere; Sonication;
99%
With 0.2C27H36N2*Pt; hydrogen; In tetrahydrofuran; at 30 ℃; for 2.8h; under 750.075 Torr; chemoselective reaction;
99%
With hydrogen; In ethanol; at 20 ℃; for 1h; under 760.051 Torr;
99%
With hydrazine hydrate; In water; at 110 ℃; Sealed tube; Green chemistry;
99%
With hydrogen; In tetrahydrofuran; ethanol; at 100 ℃; for 3h; under 7600.51 Torr; Autoclave;
97%
benzyl 4-nitrophenyl ether; With tin(II) chloride dihdyrate; In ethanol; at 70 ℃; for 6h; Inert atmosphere;
With sodium hydrogencarbonate; In ethanol; water; Inert atmosphere;
97%
With tin(II) dichloride dihydrate; In ethanol; for 4h; Reflux;
97%
With 1,1,3,3-Tetramethyldisiloxane; In ethanol; at 20 ℃; for 0.5h; Reagent/catalyst; chemoselective reaction;
97%
With hydrogen; In ethyl acetate; for 8h; under 760.051 Torr; Heating; Flow reactor; Green chemistry;
96%
With maghemite; methylhydrazine; In ethanol; at 60 ℃; for 1h; chemoselective reaction; Sealed tube; Inert atmosphere;
96%
With sodium tetrahydroborate; TPGS-750-M; In tetrahydrofuran; water; at 20 ℃; for 16h; Time;
96%
With C30H29BrMnNO2P2; hydrogen; potassium carbonate; In toluene; at 130 ℃; for 24h; under 60006 Torr; chemoselective reaction; Glovebox; Autoclave;
96%
With ethanol; tin(ll) chloride; at 65 ℃; for 1.5h;
95%
With trichlorosilane; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 0 - 20 ℃; for 18h; chemoselective reaction; Inert atmosphere;
95%
With hydrogenchloride; iron; for 1h; Heating;
95%
With iron; ammonium chloride; In water; acetone; Inert atmosphere; Reflux;
93%
With tin(ll) chloride; In ethanol; at 70 ℃; for 0.5h;
91%
With water; at 20 ℃; chemoselective reaction; Inert atmosphere;
91%
With hydrogen; In toluene; at 0 ℃; for 16h; Catalytic behavior;
91%
With palladium 10% on activated carbon; In methanol; ethanol; at 20 ℃; for 24h; under 7500.75 Torr;
90%
With tin(ll) chloride; In ethanol; at 45 ℃; for 24h; Inert atmosphere;
90.3%
With zinc phthalocyanine; hydrazine hydrate; In PEG-400; at 100 ℃; for 8h;
89%
With ethanol; sodium t-butanolate; In 1,4-dioxane; at 100 ℃; for 10h;
89%
With [Co(κS,N-4-(trifluoromethyl)pyrimidine-2-thiolate)3]; methylhydrazine; In methanol; at 70 ℃; for 5h; Sealed tube;
89%
With cobalt(II) phthalocyanine; hydrazine hydrate; In ethylene glycol; at 90 ℃; for 1.5h; chemoselective reaction;
87%
With potassium tert-butylate; isopropyl alcohol; bis(pinacol)diborane; at 110 ℃; for 2h;
87%
With iron; ammonium chloride; In tetrahydrofuran; methanol; water; at 50 ℃; for 18h;
87%
With nickel; In N,N-dimethyl-formamide; for 18h; Ambient temperature;
86%
With sodium tetrahydroborate; In methanol; water; at 0 - 50 ℃; for 3h; chemoselective reaction;
86%
With hydrogen; In methanol; ethyl acetate; at 90 ℃; for 0.333333h; chemoselective reaction; Flow reactor; Green chemistry;
85%
With C32H16FeN8*Fe(2+)*7H2O*O4S(2-); hydrazine hydrate; In ethanol; water; at 120 ℃; chemoselective reaction;
84%
benzyl 4-nitrophenyl ether; With hydrogenchloride; 1,1,1,3',3',3'-hexafluoro-propanol; iron; In water; at 20 ℃; for 0.5h;
With sodium hydrogencarbonate; In water; chemoselective reaction;
82%
With gold nanoparticles supported on titanium dioxide (TiO2); ammonium formate; In acetonitrile; at 25 ℃; for 3h; chemoselective reaction; Inert atmosphere;
81%
With hydrazine hydrate; at 100 ℃; for 0.75h; under 5171.62 Torr; chemoselective reaction; Microwave irradiation;
81%
With hydrogen; In ethanol; at 20 ℃; for 2h; under 760.051 Torr;
81%
With acetic acid; zinc; In dichloromethane; at 20 ℃;
80%
With ammonium formate; In ethylene glycol; at 120 ℃; for 12h;
75%
With iron(III) chloride hexahydrate; pyrographite; hydrazine hydrate; In ethanol; for 5h; Reflux;
75%
With hydrogenchloride; gallium; In ethanol; at 20 ℃; for 0.5h; chemoselective reaction; Sonication;
73%
With 5%-palladium/activated carbon; hydrogen; In ethanol; at 20 ℃; for 18h;
72%
With ammonia borane; gold on titanium oxide; In ethanol; at 20 ℃; for 0.833333h; Inert atmosphere;
63%
With 2-(4'-carboxyphenyl)benzothiazoline; In toluene; for 0.5h; Molecular sieve; Reflux; Inert atmosphere;
55%
With hydrazine hydrate; nickel; In methanol; for 0.166667h; Heating;
40%
With hydrazine hydrate; In ethanol; at 78 ℃; for 45h;
40%
With palladium 10% on activated carbon; ammonium formate; silica gel; In methanol; for 1.5h; Milling;
37%
With iron; acetic acid;
With nickel; isopropyl alcohol; Hydrogenation;
With nickel; hydrazine hydrate;
With hydrazine hydrate; nickel; In tetrahydrofuran;
With sodium hydroxide; carbon monoxide; <1,5-HDRhCl>2; In water; toluene; at 30 ℃; under 750.06 Torr; specific rate of reduction under biphasic condition;
With iron; ammonium chloride; acetic acid; In ethanol; at 75 ℃; for 3h;
With hydrogen; platinum on activated charcoal; In tetrahydrofuran; ethanol;
With Pd/C; hydrogen; In methanol;
With iron(III) chloride hexahydrate; pyrographite; hydrazine hydrate; In ethanol; Reflux;
With hydrazine hydrate; In ethanol; at 80 ℃; for 2h; chemoselective reaction; Inert atmosphere;
99 %Chromat.
With platinum(IV) oxide; hydrogen; In methanol; at 20 ℃; for 1h;
With sodium sulfide; In ethanol; at 25 - 80 ℃;
70 g
With iron; ammonium chloride; In ethanol; water; at 70 ℃; for 1h;
With iron; ammonium chloride; In ethanol; water; for 1h;
With iron; ammonium chloride; In ethanol; water; at 80 ℃; for 0.5h;
With sodium tetrahydroborate; In tetrahydrofuran; water; at 20 ℃; for 2h; Catalytic behavior;
99 %Chromat.
With iron; ammonium chloride; In ethanol; for 1h; Reflux;
With sodium tetrahydroborate; In water; at 20 ℃; for 0.0333333h; chemoselective reaction;
With hydrazine hydrate; In water; at 110 ℃; for 1h; Sealed tube;
With iron; ammonium chloride; In ethanol; water; Reflux;
With aluminum amalgam; water; In tetrahydrofuran; at 20 ℃; for 0.5h;
87 mg
With hydrogenchloride; iron; In ethanol; water; at 60 ℃;

2.What is the CAS number for 4-BENZYLOXYANILINE ?

The CAS number of 4-BENZYLOXYANILINE is 6373-46-2.

More information of 4-BENZYLOXYANILINE 6373-46-2 are:

CAS?Number

6373-46-2

Density

1.129 g/cm3

Melting Point

54-55 °C

Boiling Point

357.7 °C at 760 mmHg

Flash Point

180.4 °C

HS CODE

29214200

PSA

35.25000

LogP

3.42900

Pka

5.17±0.10(Predicted)

3.What are another words for 4-BENZYLOXYANILINE ?

Synonyms?for?4-BENZYLOXYANILINE 6373-46-2:p-Benzyloxyaniline;

4.What is the molecular formula of 4-BENZYLOXYANILINE?

The chemical formula of ?4-BENZYLOXYANILINE is?C13H13NO which containing 13 Carbon atoms,13 Hydrogen atoms,1 Nitrogen atoms and 1 Oxygen atoms,and the molecular weight of??4-BENZYLOXYANILINE?is 199.252.

5.What is 4-BENZYLOXYANILINE (6373-46-2) used for?

4-Benzyloxyaniline is an organic compound that serves as an intermediate in the synthesis of various pharmaceuticals and chemical compounds. It is characterized by the presence of an aniline group attached to a benzyloxy substituent, which contributes to its reactivity and potential applications in chemical synthesis.

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

Relevant articles related to 4-BENZYLOXYANILINE:

Article

Source

Chemoselective Hydrogenation of Nitroarenes Using an Air-Stable Base-Metal Catalyst

Zubar, Viktoriia,Dewanji, Abhishek,Rueping, Magnus

supporting information, p. 2742 - 2747 (2021/05/05)

Structure based design, synthesis, and biological evaluation of imidazole derivatives targeting dihydropteroate synthase enzyme

Daraji, Drashti G.,Rajani, Dhanji P.,Rajani, Smita D.,Pithawala, Edwin A.,Jayanthi, Sivaraman,Patel, Hitesh D.

supporting information, (2021/02/16)

6.Buy 4-BENZYLOXYANILINE with the best price .

Zhuhai Sanxin Fine Chemical Co., Ltd. is a quality supplier of 4-BENZYLOXYANILINE. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on 4-BENZYLOXYANILINE 6373-46-2.

Related Products