CAS No.106-51-4,1,4-Benzoquinone Suppliers,MSDS download

Jinan Finer Chemical Co., Ltd

Product description: Product name 1,4-Benzoquinone CAS number 106-51-4 Assay ≥99% Appearance Yellow crystal Capacity 500mt/year Application Dyes and pharmaceutical intermedia

1,4-Benzoquinone

Cas:106-51-4

Min.Order:100 Gram

FOB Price: $12.0

Type:Lab/Research institutions

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Lonwin Chemical Group Limited

1,4-Benzoquinone CAS: 106-51-4 Specification Product name 1,4-Benzoquinone CAS number 106-51-4 Assay ≥99% Appearance Yellow crystal Capacity 500mt/year Application Dyes and

Factory supply 1,4-Benzoquinone

Cas:106-51-4

Min.Order:1 Kilogram

Negotiable

Type:Other

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ZHIJIANG ZENVA SINO COMMERCE AND TRADE CO., LTD.

Usage: It can be widely used in medicine, herbicide, chemicals and dyes Package, storage and transportation: 1. In 35 kgs N.W. or 25 kgs N.W. cardboard drum lined with double plastic bags 2. Keep in cool, dry places under 10-20℃ and away from s

P-Benzoquinone

Cas:106-51-4

Min.Order:1 Metric Ton

Negotiable

Type:Trading Company

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Hunan Russell Chemicals Technology Co.,Ltd

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China

1,4-Benzoquinone 106-51-4

Cas:106-51-4

Min.Order:0

Negotiable

Type:Trading Company

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Suzhou Sinosun Imp.&Exp. Corporation

Water:0.5%Max; Residue on ignition:0.05%Max; Melting point: 112-116℃Appearance:yellow crystals

1,4-Benzoquinone

Cas:106-51-4

Min.Order:0

Negotiable

Type:Trading Company

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Amadis Chemical Co., Ltd.

1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G

Amadis Chemical offer CAS#106-51-4;CAT#A801452

Cas:106-51-4

Min.Order:10 Milligram

Negotiable

Type:Lab/Research institutions

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Pure Chemistry Scientific Inc.

1,4-Benzoquinone Application:814872

1,4-Benzoquinone

Cas:106-51-4

Min.Order:1 Gram

FOB Price: $500.0

Type:Trading Company

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Synthetic route

: 150-76-5
4-methoxy-phenol

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With bis-[(trifluoroacetoxy)iodo]benzene In water; acetonitrile for 0.166667h; Ambient temperature;	100%
With copper(II) nitrate/zeolite H-Y Product distribution; Further Variations:; heating mode; times; microwave irradiation;	100%
With manganese dioxide impregnated with nitric acid In dichloromethane for 0.5h; Ambient temperature;	96%

: 123-31-9
hydroquinone

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With barium ferrate(VI) In benzene for 0.25h; Product distribution; Heating;	100%
With benzyltrimethylammonium tribromide; sodium acetate In dichloromethane; water for 2h; Ambient temperature;	100%
With bis(2,2'-bipyridyl) copper(II) permanganate In dichloromethane for 0.25h; Ambient temperature;	100%

: 108-95-2
phenol

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With CuCl2 In acetonitrile	100%
With [CuII2(μ-OH)(1,2-bis(2-(bis(2-pyridylmethyl)aminomethyl)-6-pyridyl)ethane)](ClO4)3 ; dihydrogen peroxide; triethylamine In water; acetonitrile at 50℃; for 10h; Catalytic behavior; Inert atmosphere;	99%
With manganese(IV) oxide; sulfuric acid; aniline at 10℃; for 1.5h;	95%

: 123-31-9
hydroquinone

A: 36831-87-5
diphenyl-2,5 furannedicarbaldehyde 3,4

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With barium ferrate(VI) In benzene for 0.3h; Heating;	A 70% B 100%

: 150-78-7
1,4-dimethoxybezene

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With bis-[(trifluoroacetoxy)iodo]benzene In methanol; water at 20℃; for 4h;	100%
With manganese dioxide impregnated with nitric acid In dichloromethane for 1.5h; Ambient temperature;	93%
With Oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 1h;	86%

: 2117-24-0
1,4-bis(trimethylsilyloxy)benzene

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With pyridinium chlorochromate In dichloromethane at 25℃; for 2h; Mechanism; relative reaction rate;	99%
With quinolinium monofluorochromate(VI) In dichloromethane for 1h; Ambient temperature;	98%
With dioxochloro(trimethylsiloxy)chromate(VI) In dichloromethane for 0.333333h; Ambient temperature;	97%

: 99-93-4
4-Hydroxyacetophenone

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With 3-chloro-benzenecarboperoxoic acid In acetonitrile at 80℃; for 0.75h; Baeyer-Villiger Ketone Oxidation; regioselective reaction;	99%

: 106-50-3
1,4-phenylenediamine

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With sodium periodate In water at 20℃; for 0.166667h;	98%
With [bis(acetoxy)iodo]benzene In acetone at 20℃; for 0.166667h;	90%
With sulfuric acid; manganese triacetate In water at 35℃; Rate constant; Mechanism;
With dichromate anion
With manganese(IV) oxide; sulfuric acid

: 55-21-0
benzamide

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With iodobenzene; oxone; water In acetonitrile at 20℃;	98%
With sodium hydrogen sulfate; [bis(acetoxy)iodo]benzene In water; acetonitrile at 20℃; for 0.5h; Time; Solvent;	80%

: 622-62-8
4-Ethoxyphenol

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With Oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 0.5h;	97%
With bis-[(trifluoroacetoxy)iodo]benzene In water; acetonitrile for 0.166667h; Ambient temperature;	93%
With oxone; tetrabutylammomium bromide In water; acetonitrile at 20℃; for 1h;	92%
With Oxone In water; acetonitrile at 20℃; for 17h;	79%

: 51-66-1
4-methoxyacetanilide

A: 119-81-3
4-methoxy-2-nitroacetanilide

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With nitric acid; silica gel In dichloromethane for 0.166667h; Product distribution; Ambient temperature;	A 97% B 2%

: 150-78-7
1,4-dimethoxybezene

A: 89-39-4
1,4-dimethoxy-2-nitrobenzene

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With nitric acid; silica gel In dichloromethane for 0.0833333h; Product distribution; Ambient temperature;	A 97% B 2%

: 108-95-2
phenol

A: 88-89-1
2,4,6-Trinitrophenol

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With NO+18-crown-6H(NO3)2- In various solvent(s) for 2h; Nitration; Heating;	A 94% B 5%
With Zn(NO3)2*2N2O4 In ethyl acetate at 20℃; for 0.25h;	A 86% B 8%

: 122-95-2
1,4-diethoxybenzene

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With Oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 1h;	94%
With oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 1h;	94%
With ammonium cerium(IV) nitrate In water; acetonitrile at 20℃;	66%

: C24H23NO5

A: C17H17NO4

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With cerium(IV) ammonium nitrate; silica gel In water; acetonitrile at 20℃;	A 94% B n/a

: 62790-87-8
4-(tert-butyldimethylsilyloxy)anisole

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 1.5h;	94%
With Oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 1.5h;	79%

: 3424-93-9
4-methoxyphenylacetamide

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With iodobenzene; oxone; water In acetonitrile at 20℃;	94%
With sodium hydrogen sulfate; [bis(acetoxy)iodo]benzene In water; acetonitrile at 20℃; for 0.666667h;	75%

: 71-43-2
benzene

A: 106-51-4
p-benzoquinone

B: 108-95-2
phenol

Conditions

Conditions	Yield
With [CuII2(μ-OH)(1,2-bis(2-(bis(2-pyridylmethyl)aminomethyl)-6-pyridyl)ethane)](ClO4)3 ; dihydrogen peroxide; triethylamine In water; acetonitrile at 50℃; for 40h; Catalytic behavior; Inert atmosphere;	A 6.8% B 93.2%
With dihydrogen peroxide In water for 0.25h; Reagent/catalyst; Irradiation;	A n/a B 81.5%
With tetrakis(acetonitrile)copper(I) perchlorate; dihydrogen peroxide In water; acetonitrile at 25℃; for 4h; Catalytic behavior; Reagent/catalyst;	A 60% B n/a

: 123-30-8
4-amino-phenol

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With K10 montmorillonite; iodic acid for 0.00833333h; microwave irradiation;	93%
With Montmorillonite K10; iodic acid at 68℃; for 0.00555556h; microwave irradiation;	85%
With pyridine hydrogenfluoride; sodium nitrite Product distribution; Mechanism; other substrates, various temp.;	80%

: C25H23NO3

A: C17H15NO2

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With cerium(IV) ammonium nitrate; silica gel In water; acetonitrile at 20℃;	A 93% B n/a

: 52867-18-2
N-phenylsulphonyl-Se,Se-diphenylselenimide

: 123-31-9
hydroquinone

A: 98-10-2
benzenesulfonamide

B: 1132-39-4
diphenylselenide

C: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
In toluene for 25h; Product distribution; Heating; other N-sulfonylchalcogenimides, other quinones, var. solvent and time;	A 92% B 87% C 89%

...Expand

: 122-94-1
4-n-butoxyphenol

: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With oxone; tetrabutylammomium bromide In water; acetonitrile at 20℃; for 1h;	92%
With Oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 0.5h;	88%
With Oxone In water; acetonitrile at 20℃; for 17h;	77%

: C28H23NO4

A: C20H15NO3

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With cerium(IV) ammonium nitrate; silica gel In water; acetonitrile at 20℃;	A 91% B n/a

: C23H18Cl2N2O5

A: 3-(2,4-dichlorophenoxy)-4-(4-nitrophenyl)azetidin-2-one

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With cerium(IV) ammonium nitrate; silica gel In water; acetonitrile at 20℃;	A 91% B n/a

: C27H22N2O8

A: C20H16N2O7

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With cerium(IV) ammonium nitrate; silica gel In dichloromethane at 20℃;	A 90% B n/a

: 1-(4-(benzyloxy)phenyl)-3-hydroxy-2-phenoxypropan-1-one

A: 103-16-2
4-Benzyloxyphenol

B: 4-(benzyloxy)phenyl 3-hydroxy-2-phenoxypropanoate

C: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With methanesulfonic acid; dihydrogen peroxide In water; acetonitrile at 50℃; for 6h; Flow reactor; Green chemistry;	A 1% B 8% C 90%

...Expand

: C23H19NO5

: 4-(benzo[d][1,3]dioxol-5-yl)-3-phenoxyazetidin-2-one

B: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With ceric(IV) tetra-n-butylammonium nitrate; water In dichloromethane at 20℃; for 0.333333h; Reagent/catalyst; Solvent; Temperature;	A 89% B n/a

: 92409-23-9
1-(4-methoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propan-1-one

A: 4-methoxyphenyl 3-hydroxy-2-(2-methoxyphenoxy)propanoate

B: 150-76-5
4-methoxy-phenol

C: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With methanesulfonic acid; dihydrogen peroxide In water; acetonitrile at 50℃; for 6h; Flow reactor; Green chemistry;	A 9% B 2% C 89%

...Expand

: 108-24-7
acetic anhydride

: 106-51-4
p-benzoquinone

: 613-03-6
1,2,4-triacetoxybenzene

Conditions

Conditions	Yield
With sulfuric acid at 40 - 50℃;	100%
With sulfuric acid at 10 - 45℃; for 1h;	97.4%
With sulfuric acid at 25 - 50℃; for 0.5h; Reagent/catalyst; Temperature;	96%

: 542-92-7
cyclopenta-1,3-diene

: 106-51-4
p-benzoquinone

: 51175-59-8
norbornenoquinone

Conditions

Conditions	Yield
In hexane; ethyl acetate at 0℃; for 3.5h; Diels-Alder Cycloaddition;	100%
In methanol at -78 - 0℃; Inert atmosphere; optical yield given as %de;	98%
In hexane; ethyl acetate at 0℃; for 4h; Diels-Alder reaction;	97%

: 106-51-4
p-benzoquinone

: 5273-62-1
5,6-dichlorocyclohex-2-ene-1,4-dione

Conditions

Conditions	Yield
With sulfuryl dichloride; triethylamine In diethyl ether for 0.5h;	100%
With chloroform; chlorine
With sulfuryl dichloride

: 106-51-4
p-benzoquinone

: 123-31-9
hydroquinone

Conditions

Conditions	Yield
With nickel In tetrahydrofuran at 20℃; for 0.166667h; Reduction;	100%
With boron trifluoride diethyl etherate; sodium iodide In acetonitrile at 0℃; for 0.0833333h;	99%
With hydrazine hydrate In acetonitrile at 20℃; for 18h; Irradiation;	99%

: 1613-51-0
sulfure de pentamethylene

: 106-51-4
p-benzoquinone

: 2,5-dihydroxyphenylthianium perchlorate

Conditions

Conditions	Yield
With perchloric acid In acetone at 0℃;	100%

: 1613-51-0
sulfure de pentamethylene

: 106-51-4
p-benzoquinone

: 89706-15-0
1-(2,5-dihydroxyphenyl)thianium bromide

Conditions

Conditions	Yield
With hydrogen bromide In acetone at 0℃;	100%

: 542-92-7
cyclopenta-1,3-diene

: 106-51-4
p-benzoquinone

: 78548-82-0
1α,4α,4aβ,10aα,5β,8β,8aα,9aβ-octahydro-1,4:5,8-dimethanoanthracene-9,10-dione

Conditions

Conditions	Yield
In benzene at 40℃; for 20h;	100%
In dichloromethane at 20℃; for 24h; Diels-Alder reaction;	100%
In ethanol at 0℃; for 0.5h; Diels-Alder Cycloaddition;	98%

: 108-98-5
thiophenol

: 106-51-4
p-benzoquinone

: 18231-96-4
2-(phenylthio)benzene-1,4-diol

Conditions

Conditions	Yield
In methanol	100%
With methanol at 20℃; for 6h;	99%
In methanol for 0.166667h; Ambient temperature;	95%

: 4559-70-0
Diphenylphosphine oxide

: 106-51-4
p-benzoquinone

: 13291-46-8
(2,5-dihydroxyphenyl)diphenylphosphine oxide

Conditions

Conditions	Yield
In toluene for 1.66667h;	100%
With water In toluene at 80℃; for 12h; Inert atmosphere; Schlenk technique;	98%
In toluene for 20h; Inert atmosphere; Reflux;	88.1%
In toluene at 75 - 110℃; for 1h; Michael Addition; Inert atmosphere;	86%
In toluene

: 781-43-1
9,10-dimethylanthracene

: 106-51-4
p-benzoquinone

: 115163-71-8
9,10-Dimethyl-12,15-dioxo-11,12,15,16-tetrahydro-triptycen

Conditions

Conditions	Yield
With magnesium(II) perchlorate In acetonitrile at 24.9℃; dependence of kobs on ;	100%
With magnesium(II) perchlorate In acetonitrile	100%
In chloroform-d1 at 24.85℃; Quantum yield;	65%
With p-benzoquinone*2thymol eutectic for 0.5h; Diels-Alder reaction;	95 % Spectr.
With magnesium(II) perchlorate In [D3]acetonitrile at 24.84℃; Kinetics; Further Variations:; Reagents; Diels-Alder reaction;

: 33862-44-1
diphenyl phosphorohydrazidate

: 106-51-4
p-benzoquinone

: C18H15N2O4P

Conditions

Conditions	Yield
In benzene at 25℃;	100%

: 20742-48-7
cis-3-thiabicyclo<3.3.1>nonane

: 106-51-4
p-benzoquinone

: (1R,5S)-3-(2,5-Dihydroxy-phenyl)-3-thionia-bicyclo[3.3.1]nonane; hydrogen sulfate

Conditions

Conditions	Yield
With sulfuric acid In acetone at 0℃;	100%

: 88888-43-1
(E)-8-Nitro-octa-1,3-diene

: 106-51-4
p-benzoquinone

: (4aR,5R,8aS)-5-(4-Nitro-butyl)-4a,5,8,8a-tetrahydro-[1,4]naphthoquinone

Conditions

Conditions	Yield
In toluene at 110℃; for 15h;	100%

: 106-51-4
p-benzoquinone

: 637-88-7
1,4-Cyclohexanedione

Conditions

Conditions	Yield
With aluminium trichloride; zinc In tetrahydrofuran for 0.4h; Ambient temperature;	100%
With formic acid In toluene at 120℃; for 10h; Inert atmosphere; chemoselective reaction;	57%
With hydrogen; tetra-(n-butyl)ammonium iodide In water at 110℃; under 15001.5 Torr; for 24h; chemoselective reaction;	57%
With ruthenium; hydrogen at 80℃; under 37503.8 Torr; for 1h; Reagent/catalyst; Ionic liquid; chemoselective reaction;

: 73296-31-8
phenyltellurotrimethylsilane

: 106-51-4
p-benzoquinone

: 2117-24-0
1,4-bis(trimethylsilyloxy)benzene

Conditions

Conditions	Yield
In tetrahydrofuran at 20℃; for 0.5h; reductive silylation;	100%

: 106-51-4
p-benzoquinone

: 270589-03-2
(E,E)-2-pyridyldimethyl(buta-1,3-dienyl)silane

: 130-15-4
[1,4]naphthoquinone

Conditions

Conditions	Yield
With hydrogenchloride In water at 20℃; for 38h;	100%
With hydrogenchloride In water at 20℃; for 38h; Product distribution; Further Variations:; Reagents; Solvents; Diels-Alder reaction;	100%

: 106-51-4
p-benzoquinone

: 270589-04-3
(E,E)-2-pyridyldimethyl(3-methylbuta-1,3-dienyl)silane

: 605-93-6
6-methyl-1,4-naphthoquinone

Conditions

Conditions	Yield
With hydrogenchloride In water at 20℃; for 38h;	100%
With hydrogenchloride In water at 20℃; for 38h; Diels-Alder reaction;	100%

: tetrafluoroboric acid

: 1273-94-5
1,1'-diacetylferrocene

: 106-51-4
p-benzoquinone

: 1,1'-diacetylferriceniumtetra-fluoroborate

Conditions

Conditions	Yield
In diethyl ether; chloroform Dropwise addn. (Ar) of ferrocene complex in dry chloroform to org. compd. in the presence of HBF4 (Et2O) at -10°C, and stirring (1 h, room temp.) of resulting soln.; Isolation of resulting compd. by filtn. and silica gel chromy.;	100%

...Expand

: 117226-57-0
1,3-bis(trimethylsilyl)-1,3-diaza-2-germa(II)indane

: 106-51-4
p-benzoquinone

: 2C6H4(N(Si(CH3)3))2(2-)*2Ge(3+)*(OC6H4O)(2-)

Conditions

Conditions	Yield
In toluene monomer feed ratio germylene : p-benzoquinone = 4.0 : 1.0, at -78°C under Ar for 1 h; elem. anal.;	100%
In tetrahydrofuran monomer feed ratio germylene : p-benzoquinone = 2.0 : 1.0, at -78°C under Ar for 1 h; elem. anal.;	96%
In toluene monomer feed ratio germylene : p-benzoquinone = 2.0 : 1.0, at -78°C under Ar for 1 h; elem. anal.;	91%
In toluene monomer feed ratio germylene : p-benzoquinone = 1.0 : 1.0, at -78°C under Ar for 1 h; elem. anal.;	86%

: bis(β-dimethylaminoethoxy)tin

: 106-51-4
p-benzoquinone

: Sn(OCH2CH2N(CH3)2)2(OC6H4O)

Conditions

Conditions	Yield
In benzene under N2, soln. of C6H4O2 in benzene added to Sn compd. in benzene at 22-24°C, refluxed with stirring for 2 h; ppt. filtered off, washed with benzene, dried; elem. anal.;	100%

: 59863-12-6
bis[bis(trimethylsilyl)amino]germanium(II)

: 106-51-4
p-benzoquinone

: Ge(N(Si(CH3)3)2)2OC6H4O

Conditions

Conditions	Yield
In benzene (Ar); stirring (1 h, 25°C); soln. filtn. off, drying (vac.);	100%
In toluene (Ar); stirring (1 h, -78, 0 or 50°C); soln. filtn. off, drying (vac.); elem. anal.;	100%
In diethyl ether (Ar); stirring (1 h, 0°C); soln. filtn. off, drying (vac.);	99%

: 14221-01-3
tetrakis(triphenylphosphine) palladium(0)

: 106-51-4
p-benzoquinone

: 490039-51-5, 57036-58-5
[palladium(0)(triphenylphosphine)2(p-benzoquinone)]

Conditions

Conditions	Yield
In benzene under N2 atm. to suspn. Pd(PPh3)4 in benzene was added soln. benzoquinone in benzene and stirred for 30 min; soln. was concd., ether-hexane was added;	100%

pine pitch: pine pitch

: 106-51-4
p-benzoquinone

: (4aR,4bS,7R,10aR,10bS,12R,12aR)-13-isopropyl-7,10a-dimethyl-1,4-dioxo-4,4a,5,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-4b,12-ethenochrysene-7-carboxylic acid