CAS No.127-08-2,Potassium acetate Suppliers,MSDS download

Dayang Chem (Hangzhou) Co.,Ltd.

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Suzhou Sinosun Imp.&Exp. Corporation

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Yixing Zeyuan Chemical Technology Co Ltd

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Jinan Finer Chemical Co., Ltd

Product Description Name Potassium acetate CAS 127-08-2 Assay ≥98%, 30%, 40%, 50% Appearance White crystalline powder or liquid Capacity 3000mt/year Min.package 100gram

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Wuhan Fortuna Chemical Co.,Ltd

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Ality Chemical Corporation

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EAST CHEMSOURCES LIMITED

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Xi'an Xszo Chem Co., Ltd.

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COLORCOM LTD.

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Chongqing Changfeng Chemical Co., Ltd.

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Henan Tianfu Chemical Co., Ltd.

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Hebei Nengqian Chemical Import and Export Co., LTD

With our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufactu

CAS: 127-08-2 Potassium Acetate

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Zhuozhou Wenxi import and Export Co., Ltd

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Hebei Sankai Chemical Technology Co., Ltd

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Wuhan Han Sheng New Material Technology Co.，Ltd

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Hot Sell Factory Supply Raw Material CAS 127-08-2 Potassium Acetate

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Henan Sinotech Import&Export Corporation

1. Chemical Name: Potassium acetate 2. Molecular Formula : C2H3KO2 3. Molecular Weight: 98.14 4. CAS: 127-08-2 5. Character: It is white crystalline powder. It is deliquescent and tastes salty.Relative density is 1.570. Melting point i

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Hubei Langyou International Trading Co., Ltd

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Shanghai Minstar Chemical Co., Ltd

Product Name: Potassium Acetate CAS: 127-08-2 MF: C2H3KO2 MW: 98.14 EINECS: 204-822-2 Mol File: 127-08-2.mol Potassium Acetate Structure Potassium Acetate Chemical Properties Melting point 292 °C density 1.57 g/cm3 at

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Qingdao Beluga Import and Export Co., LTD

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Shandong Hanjiang Chemical Co., Ltd.

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Leader Biochemical Group

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Lonwin Chemical Group Limited

Potassium acetate CAS: 127-08-2 Specification Name Potassium acetate CAS 127-08-2 Assay ≥98%, 30%, 40%, 50% Appearance White crystalline powder or liquid Capacity 3000mt/year

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Henan Wentao Chemical Product Co., Ltd.

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Wuhan Zenuo Biological Medicine Technology Co Ltd

Product Name: Potassium Acetate Synonyms: Potassium acetate 99.98% trace metals basis, ~100 ppm Rb, <50 ppm Cs;Potassium acetate ACS reagent, >=99.0%;Potassium acetate anhydrous, free-flowing, Redi-Dri(TM), ACS reagent, >=99.0%;Potassiu

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Synthetic route

: potassium 3-(bis[(N'-tert-butylureaylato)-N-ethyl]aminatomethyl)-5-tert-butyl-1H-pyrazolato(hydroxo)cobaltate(II) N,N-dimethylacetamide adduct (1/2)

: 141-78-6
ethyl acetate

: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In diethyl ether; N,N-dimethyl acetamide; ethyl acetate (Ar); vapor diffusion of Et2O into a (CH3)2NCOCH3/EtOAc soln. of Co complex;	100%
In N,N-dimethyl acetamide; ethyl acetate (Ar); stirred for 2 h at room temp.;

: 127-19-5
N,N-dimethyl acetamide

: 1159806-92-4
bis[(N'-isopropylureido)-N-ethyl]-N-methylamine

: 7732-18-5
water

: 373-02-4, 14998-37-9, 33025-09-1, 94044-50-5, 98268-31-6
nickel diacetate

: potassium hydride

: 1159806-63-9
K[Ni(bis[(N'-isopropylureido)-N-ethyl]-N-methylamine(-2H))(hydroxo)]*DMA

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In N,N-dimethyl acetamide (Ar); treatment of soln. of urea deriv. in dimethylacetamide with 2 equiv. of KH at room temp., addn. of 1 equiv. of nickel compd. at room temp., filtration, addn. of 1 equiv. of KH, addn. of 1 equiv. of water; evapn., triturating with ether, isolation of ppt., IR and UV;	A n/a B 99%
In N,N-dimethyl acetamide (Ar); treatment of soln. of urea deriv. in dimethylacetamide with 3 equiv. of KH at room temp., addn. of 1 equiv. of nickel compd. at room temp., stirring for 45 min, addn. of 1 equiv. of water, stirring for 20 min; filtration, diffusion of 1:1 ether/pentane vapour, isolation of crystals, elem. anal.;	A 64% B 98%

...Expand

: 127-19-5
N,N-dimethyl acetamide

: 1000006-56-3
3-(bis[(N'-tert-butylureaylato)-N-ethyl]aminatomethyl)-5-tert-butyl-1H-pyrazole

: 7732-18-5
water

: 71-48-7, 917-69-1, 5931-89-5, 55881-15-7, 68931-68-0, 68931-69-1, 93029-27-7
cobalt(II) acetate

: potassium hydride

: potassium 3-(bis[(N'-tert-butylureaylato)-N-ethyl]aminatomethyl)-5-tert-butyl-1H-pyrazolato(hydroxo)cobaltate(II) N,N-dimethylacetamide adduct (1/2)

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In N,N-dimethyl acetamide (Ar); a soln. of ligand treated with KH, Co salt added, stirred for 30 min, filtered, H2O added, stirred for 30 min; evapd. (vac., at room temp.), washed (Et2O), dried (vac.); elem. anal.;	A 83% B 98%

...Expand

: 1159806-63-9
K[Ni(bis[(N'-isopropylureido)-N-ethyl]-N-methylamine(-2H))(hydroxo)]*DMA

: 10581-12-1
tetramethyl ammonium acetate

: 40949-94-8
potassium hexamethylsilazane

A: [Ni(bis[(N'-isopropylureido)-N-ethyl]-N-methylamine(-2H))(oxo)](2-)

: [tetramethylammonium]0.5K0.5[Ni(bis[(N'-isopropylureido)-N-ethyl]-N-methylamine(-2H))(OSiMe3)]*DMA

C: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In N,N-dimethyl acetamide (Ar); treatment of soln. of nickel compd. in dimethylacetamide with 1 equiv. of potassium amide deriv. at room temp., stirring for 30 min, addn.of tetramethylammonium salt at room temp., stirring for 1 h; filtration, evapn., triturating with diethyl ether, isolation of ppt., recrystn. by diffusion of 1:1 diethyl ether/pentane vapour into soln. in dimethylacetamide, elem. anal.;	A 0% B 94% C 98%

Yield

In N,N-dimethyl acetamide (Ar); treatment of soln. of nickel compd. in dimethylacetamide with 1 equiv. of potassium amide deriv. at room temp., stirring for 30 min, addn.of tetramethylammonium salt at room temp., stirring for 1 h; filtration, evapn., triturating with diethyl ether, isolation of ppt., recrystn. by diffusion of 1:1 diethyl ether/pentane vapour into soln. in dimethylacetamide, elem. anal.;

A 0%
B 94%
C 98%

...Expand

: 1159806-68-4
K[Ni(bis[(N'-tert-butylureido)-N-ethyl]-N-methylamine(-2H))(hydroxo)]*DMA

: 865-47-4
potassium tert-butylate

: 10581-12-1
tetramethyl ammonium acetate

A: [Ni(bis[(N'-tert-butylureido)-N-ethyl]-N-methylamine(-2H))(oxo)](2-)

B: 1159806-80-0
[tetramethylammonium][Ni(bis[(N'-tert-butylureido)-N-ethyl]-N-methylamine(-2H))(tert-butoxide)]

C: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In N,N-dimethyl acetamide (Ar); treatment of soln. of nickel compd. in dimethylacetamide with 1 equiv. of potassium tert-butoxide at room temp., stirring for 30 min, addn. of tetramethylammonium salt at room temp., stirring for 1 h; filtration, evapn., triturating with diethyl ether, isolation of ppt., recrystn. by diffusion of diethyl ether vapour into soln. in dimethylacetamide, IR and UV;	A 0% B 78% C 96%

...Expand

: 1159806-68-4
K[Ni(bis[(N'-tert-butylureido)-N-ethyl]-N-methylamine(-2H))(hydroxo)]*DMA

: 10581-12-1
tetramethyl ammonium acetate

: 40949-94-8
potassium hexamethylsilazane

A: [Ni(bis[(N'-tert-butylureido)-N-ethyl]-N-methylamine(-2H))(oxo)](2-)

B: 1159806-88-8
[tetramethylammonium][Ni(bis[(N'-tert-butylureido)-N-ethyl]-N-methylamine(-2H))(OSiMe3)]

C: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In N,N-dimethyl acetamide (Ar); treatment of soln. of nickel compd. in dimethylacetamide with 1 equiv. of potassium amide deriv. at room temp., stirring for 30 min, addn.of tetramethylammonium salt at room temp., stirring for 1 h; filtration, evapn., triturating with diethyl ether, isolation of ppt., recrystn. by diffusion of 1:1 diethyl ether/pentane vapour into soln. in dimethylacetamide, IR and UV;	A 0% B 95% C n/a

Yield

A 0%
B 95%
C n/a

...Expand

: 1159806-92-4
bis[(N'-isopropylureido)-N-ethyl]-N-methylamine

: 865-47-4
potassium tert-butylate

: 10581-12-1
tetramethyl ammonium acetate

: 373-02-4, 14998-37-9, 33025-09-1, 94044-50-5, 98268-31-6
nickel diacetate

: 1159806-75-3
[tetramethylammonium][Ni(bis[(N'-isopropylureido)-N-ethyl]-N-methylamine(-2H))(tert-butoxide)]

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
With KH In N,N-dimethyl acetamide (vac. or Ar); treatment of soln. of urea deriv. in dimethylacetamide with KH, addn. of nickel compd., stirring for 45 min, addn. of potassium tert-butoxide, addn. of tetramethylammonium salt, stirring for 1 h; evapn. triturating with diethyl ether, isolation of ppt., elem. anal.;	A 91% B 89%

...Expand

: 1159806-63-9
K[Ni(bis[(N'-isopropylureido)-N-ethyl]-N-methylamine(-2H))(hydroxo)]*DMA

: 865-47-4
potassium tert-butylate

: 10581-12-1
tetramethyl ammonium acetate

A: [Ni(bis[(N'-isopropylureido)-N-ethyl]-N-methylamine(-2H))(oxo)](2-)

: 1159806-75-3
[tetramethylammonium][Ni(bis[(N'-isopropylureido)-N-ethyl]-N-methylamine(-2H))(tert-butoxide)]

C: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In N,N-dimethyl acetamide (Ar); treatment of soln. of nickel compd. in dimethylacetamide with 1 equiv. of potassium tert-butoxide at room temp., stirring for 30 min, addn. of tetramethylammonium salt at room temp., stirring for 1 h; filtration, evapn., triturating with diethyl ether, isolation of ppt., recrystn. by diffusion of 1:1 ether/pentane vapour into soln. in dimethylacetamide, IR and UV;	A 0% B 91% C 89%

...Expand

: 127-19-5
N,N-dimethyl acetamide

: 7732-18-5
water

: 373-02-4, 14998-37-9, 33025-09-1, 94044-50-5, 98268-31-6
nickel diacetate

: potassium hydride

: 613221-93-5
bis[(N'-tert-butylureido)-N-ethyl]-N-methylamine

: 1159806-68-4
K[Ni(bis[(N'-tert-butylureido)-N-ethyl]-N-methylamine(-2H))(hydroxo)]*DMA

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In N,N-dimethyl acetamide (Ar); treatment of soln. of urea deriv. in dimethylacetamide with 3 equiv. of KH at room temp., addn. of 1 equiv. of nickel compd. at room temp., stirring for 45 min, addn. of 1 equiv. of water, stirring for 20 min; filtration, diffusion of 1:1 ether/pentane vapour, isolation of crystals, elem. anal.;	A 87% B 84%

...Expand

: potassium hydroxide

: 74-86-2
acetylene

: 127-08-2
potassium acetate

Conditions

Conditions	Yield
With water In melt byproducts: H2; 300°C, mixing, leading H2O vapor into the melt;	83%
With H2O In melt byproducts: H2; 300°C, mixing, leading H2O vapor into the melt;	83%
With air In water handling with air in presence of dild. aq. KOH in diffuse daylight at ambient temp.;
With air In water handling with air in presence of dild. aq. KOH in diffuse daylight at ambient temp.;

: 540-88-5
acetic acid tert-butyl ester

: 10519-96-7
potassium trimethylsilonate

: 127-08-2
potassium acetate

Conditions

Conditions	Yield
	77%

: 64-17-5
ethanol

: 127-08-2
potassium acetate

Conditions

Conditions	Yield
With C15H27Br2CoN3; potassium hydroxide In toluene at 140℃; for 16h; Cannizzaro Reaction; Inert atmosphere; Sealed tube;	67%

: O-acetyl-N-methoxyacetyl-hydroxylamine; potassium-compound

A: 127-08-2
potassium acetate

B: 6427-21-0
methoxymethyl isocyanate

Conditions

Conditions	Yield
at 100℃;

: 64-19-7
acetic acid

: 127-08-2
potassium acetate

Conditions

Conditions	Yield
With potassium carbonate
Stage #1: acetic acid With potassium hydroxide Electric arc; Stage #2: at 40 - 250℃;

: 28562-53-0
4-acetoxy azetidinone

A: 127-08-2
potassium acetate

B: Potassium; (E)-2-carbamoyl-ethenolate

Conditions

Conditions	Yield
With potassium hydroxide at 25℃; Mechanism; Rate constant;

: 3234-54-6
vinyl crotonate

: 1600-27-7
mercury(II) diacetate

A: 107-93-7
(E)-but-2-enoic acid

B: 127-08-2
potassium acetate

C: 5321-77-7
(formylmethyl)mercury chloride

Conditions

Conditions	Yield
With potassium chloride 1.) water, 26 deg C; 2.) water; Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: 764-48-7
2-hydroxyethyl vinyl ether

A: 497-26-7
2-methyl-1,3-dioxolane

B: 34557-54-5
methane

C: 74-84-0
ethane

D: 74-98-6
propane

E: 127-08-2
potassium acetate

F: 74-86-2
acetylene

Conditions

Conditions	Yield
With potassium hydroxide at 170℃; Product distribution; other hydroxides (Na, Li);

...Expand

: 1124-31-8
potassium 4-nitrophenolate

: 108-24-7
acetic anhydride

A: 127-08-2
potassium acetate

B: 830-03-5
4-nitrophenol acetate

Conditions

Conditions	Yield
With 18-crown-6 ether In acetonitrile at 20℃; Rate constant; Equilibrium constant;
With 18-crown-6 ether In chlorobenzene at 25℃; Rate constant; Equilibrium constant;
In acetonitrile at 25℃; Kinetics; Equilibrium constant;

...Expand

: 14314-69-3
potassium 2,4-dinitrophenolate

: 108-24-7
acetic anhydride

A: 127-08-2
potassium acetate

B: 4232-27-3
2,4-dinitrophenyl acetate

Conditions

Conditions	Yield
With 18-crown-6 ether In acetonitrile at 20℃; Rate constant; Equilibrium constant;
With 18-crown-6 ether In chlorobenzene at 25℃; Rate constant; Equilibrium constant;

...Expand

: 108-24-7
acetic anhydride

: 58765-11-0
4-hydroxybenzaldehyde potassium salt

A: 878-00-2
4-formylphenyl acetate

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
With 18-crown-6 ether In acetonitrile at 20℃; Rate constant;

...Expand

: 108-24-7
acetic anhydride

: 81409-00-9
potassium salt of p-nitrosophenol

A: 127-08-2
potassium acetate

B: 83154-99-8
Acetic acid 4-nitroso-phenyl ester

Conditions

Conditions	Yield
With 18-crown-6 ether In acetonitrile at 20℃; Rate constant;

...Expand

: 136825-69-9
di(4-acetoxybenzyl) methylphosphonate

A: 623-05-2
(4-hydroxyphenyl)methanol

B: 127-08-2
potassium acetate

C: potassium 4-acetoxybenzyl methylphosphonate

Conditions

Conditions	Yield
In [D3]acetonitrile; water-d2 at 36.4℃; Mechanism; Rate constant; potassium phosphate buffer; half-live; also in the presence of porcine liver carboxyesterase;

...Expand

: 1124-31-8
potassium 4-nitrophenolate

: 64-19-7
acetic acid

A: 100-02-7
4-nitro-phenol

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In acetonitrile at 20℃; Equilibrium constant; Further equilibria;
In acetonitrile Equilibrium constant;

...Expand

: 81409-00-9
potassium salt of p-nitrosophenol

: 64-19-7
acetic acid

A: 104-91-6
p-nitrosophenol

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
In acetonitrile at 20℃; Equilibrium constant; Further equilibria;

...Expand

: 144758-70-3
di(4-acetoxybenzyl) methoxycarbonylmethylphosphonate

A: 623-05-2
(4-hydroxyphenyl)methanol

B: 127-08-2
potassium acetate

C: C12H14O7P(1-)*K(1+)

Conditions

Conditions	Yield
In [D3]acetonitrile; water-d2 at 37℃; Mechanism; potassium phosphate buffer, porcine liver carboxyesterase; half-live; also with human plasma;

...Expand

: potassium 4-acetoxybenzyl methylphosphonate

A: 623-05-2
(4-hydroxyphenyl)methanol

B: 127-08-2
potassium acetate

C: 3999-19-7, 77354-28-0
dipotassium methylphosphonate

Conditions

Conditions	Yield
In [D3]acetonitrile; water-d2 at 36.4℃; Mechanism; Rate constant; potassium phosphate buffer; half-live; also in the presence of porcine liver carboxyesterase;

...Expand

: 144965-55-9
lithium 4-acetoxybenzyl methoxycarbonylmethylphosphonate

A: 623-05-2
(4-hydroxyphenyl)methanol

B: 127-08-2
potassium acetate

C: 144965-64-0
C3H5O5P(2-)*2K(1+)

Conditions

Conditions	Yield
In [D3]acetonitrile; water-d2 at 37℃; Mechanism; potassium phosphate buffer, porcine liver carboxyesterase; half-live; also with human plasma and with S9 fraction of porcine brain; also without any enzyme (velocity constant);

...Expand

: C8H6N3O8(1-)*K(1+)

A: 99-35-4
1,3,5-trinitrobenzene

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
With 18-crown-6 ether In acetonitrile at 15℃; Equilibrium constant; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.);

: 108-24-7
acetic anhydride

: 58200-72-9
potassium salt of 2,3,5-trichlorophenol

A: 127-08-2
potassium acetate

B: 61925-88-0
2,3,5-trichlorophenol acetate

Conditions

Conditions	Yield
With 18-crown-6 ether In chlorobenzene at 25℃; Rate constant; Equilibrium constant;
In acetonitrile at 25℃; Kinetics; Equilibrium constant;

...Expand

: 108-24-7
acetic anhydride

: 2-chloro-4-nitrophenol potassium salt

A: 18855-84-0
2-chloro-4-nitrophenyl acetate

B: 127-08-2
potassium acetate

Conditions

Conditions	Yield
With 18-crown-6 ether In chlorobenzene at 25℃; Rate constant; Equilibrium constant;
In acetonitrile at 25℃; Kinetics; Equilibrium constant;

...Expand

: 127-08-2
potassium acetate

: 100-44-7
benzyl chloride

: 140-11-4
Benzyl acetate

Conditions

Conditions	Yield
Amberlyst A27 In toluene at 95℃; for 20h;	100%
With dicyclohexano-18-crown-6 In acetonitrile at 60℃; for 0.5h; Product distribution; further reagents;	85.4%
With zirconium (benzyldiethylammoniomethylphosphonate chloride) phosphate In water; toluene at 88℃; for 15h;	82.5%

: 127-08-2
potassium acetate

: 100-11-8
1-bromomethyl-4-nitro-benzene

: 619-90-9
4-nitrobenzyl acetate

Conditions

Conditions	Yield
5,11,17,23,29,35-Hexa-p-tert-butyl-37,38,39,40,41,42-hexakis-(3,6,9-trioxadecyloxy)calix<6>arene In dichloromethane at 40℃; for 24h;	100%
5,11,17,23,29,35-Hexa-p-tert-butyl-37,38,39,40,41,42-hexakis-(3,6,9-trioxadecyloxy)calix<6>arene In dichloromethane; water at 40℃; for 24h;	100%
"octopus-type" calixarene 1 In dichloromethane; water at 40℃; for 24h; Product distribution; other catalysts, content of water, other carboxylates;	100%
With ethanol
5,11,17,23,29,35-hexa-....-calix<6>arene In dichloromethane at 40℃; for 24h; influence of other catalysts;

: 86-87-3
naphth-1-yl acetic acid

: 127-08-2
potassium acetate

: 13098-88-9
naphthalen-1-ylmethyl acetate

Conditions

Conditions	Yield
With dipotassium peroxodisulfate; copper diacetate In acetic acid for 2h; Heating;	100%

: 111-83-1
1-bromo-octane

: 127-08-2
potassium acetate

: 112-14-1
n-octyl acetate

Conditions

Conditions	Yield
Sucrose-ethyleneoxide adducts In acetonitrile at 83℃; for 24h; Product distribution; further catalysts: PEG, DB18K6; further objects of study: phase-transfer catalysis; further solvents: toluene/H2O;	100%
With aluminum oxide at 196℃; for 0.0333333h; Irradiation; other long chain halides;	99%
With aluminum oxide at 196℃; for 0.0333333h; Irradiation;	99%

: 37803-02-4
(S)-2,2'-bis(bromomethyl)-1,1'-binaphthyl

: 127-08-2
potassium acetate

: 98834-92-5
(S)-2,2'-Bis-1,1'-binaphthyl

Conditions

Conditions	Yield
With tetrabutylammomium bromide In N,N-dimethyl-formamide at 80℃; for 20h;	100%
With tetrabutylammomium bromide In N,N-dimethyl-formamide at 80℃;

: 127-08-2
potassium acetate

: 107437-25-2
methyl <1S-<1α,2α(Z),3α,4α>>-7-<3-<(tosyloxy)methyl>-7-oxabicyclo<2.2.1>hept-2-yl>-5-heptanoate

: 119785-38-5
Methyl <1S-<1α,2α(Z),3α,4α>>-7-<3-<<(2-Oxo-2-ethyl)thio>methyl>-7-oxabicyclo<2.2.1>hept-2-yl>-5-heptenoate

Conditions

Conditions	Yield
In tetrahydrofuran; dimethyl sulfoxide at 75℃; for 1.25h;	100%

: 127-08-2
potassium acetate

: endo-5,6-dimethylidene-2-norbornyl brosylate

A: (3-methylidene-2-nortricyclyl)methyl acetate

: 5,6-dimethylidene-2exo-norbornyl alcohol acetate

Conditions

Conditions	Yield
With acetic anhydride for 96h; Yields of byproduct given;	A 100% B n/a
With acetic anhydride In acetic acid at 25℃; for 72h; Yield given. Yields of byproduct given;

...Expand

: 127-08-2
potassium acetate

: C9H16ClN2O2

: 2,2,6,6-tetramethyl-3-acetoxy-4-oximinopiperidin-1-oxyl

Conditions

Conditions	Yield
In acetone for 1h;	100%

: 127-08-2
potassium acetate

: 100-39-0
benzyl bromide

: 140-11-4
Benzyl acetate

Conditions

Conditions	Yield
Sucrose-ethyleneoxide adducts In acetonitrile at 20℃; for 8h; Product distribution; further catalysts: PEG, DB18K6; further objects of study: phase-transfer catalysis; further solvents: toluene/H2O;	100%
With ammonium salt In neat (no solvent) for 2h; Ambient temperature;	99%
With tetradecane; potassium acetate; magnetic nanoparticle-supported crown ether In toluene at 80℃; for 8h;	96%

: 129236-97-1
1,4-bis(decyloxy)benzene

: 127-08-2
potassium acetate

: 444308-62-7
Acetic acid 4-acetoxymethyl-2,5-bis-decyloxy-benzyl ester

Conditions

Conditions	Yield
With tetrabutylammomium bromide In chloroform; acetonitrile Heating;	100%

: 127-08-2
potassium acetate

: 136682-02-5
3-bromo-7-hydroxymethyl-9-fluorenone

Conditions

Conditions	Yield
With sodium methylate In tetrahydrofuran; methanol for 1.25h; Ambient temperature;	100%

: 127-08-2
potassium acetate

: 685539-84-8
D-3-O-trifluoromethanesulfonyl-1,2:4,5-di-O-isopropylidene-myo-inositol

: 685539-85-9
1L-1-O-acetyl-2,3:5,6-di-O-isopropylidene-chiro-inositol

Conditions

Conditions	Yield
In N,N-dimethyl acetamide at 70℃;	100%

: 127-08-2
potassium acetate

: 685539-87-1
D-3,6-di-O-trifluoromethanesulfonyl-1,2:4,5-di-O-isopropylidene-myo-inositol

: 685539-88-2
(D)-2,5-di-O-acetyl-1,6:3,4-di-O-isopropylidene-allo-inositol

Conditions

Conditions	Yield
In N,N-dimethyl acetamide at 70℃;	100%

: 127-08-2
potassium acetate

: 232944-74-0
(3Z)-3-(chloromethyl)-4-(4-chlorophenyl)but-3-en-2-one

: Acetic acid 2-[1-(4-chloro-phenyl)-meth-(E)-ylidene]-3-oxo-butyl ester

Conditions

Conditions	Yield
With 1-n-butyl-methylimidazolium tetrafluoroborate at 45 - 50℃; for 2h;	100%

: 127-08-2
potassium acetate

: (Z)-3-Chloromethyl-4-(4-fluoro-phenyl)-but-3-en-2-one

: Acetic acid 2-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-3-oxo-butyl ester

Conditions

Conditions	Yield
With 1-n-butyl-methylimidazolium tetrafluoroborate at 45 - 50℃; for 2h;	100%

: 127-08-2
potassium acetate

: (+/-)-1,2:4,5-di-O-isopropylidene-3-O-trifluorometnanesulfonyl-myo-inositol

: rac-1-O-acetyl-2,3:5,6-di-O-isopropylidene-chiro-inositol

Conditions

Conditions	Yield
In N,N-dimethyl acetamide at 70℃;	100%

: 4-(tert-butyl)-2,6-bis(phenylazo)benzyl bromide

: 127-08-2
potassium acetate

: 4-(tert-butyl)-2,6-bis(phenylazo)benzyl acetate

Conditions

Conditions	Yield
In acetone; acetonitrile for 0.75h;	100%

: 58579-54-7
3-bromo-2-(bromomethyl)-1-nitrobenzene

: 127-08-2
potassium acetate

: 861106-90-3
2-bromo-6-nitrobenzyl acetate

Conditions

Conditions	Yield
In DMF (N,N-dimethyl-formamide) at 70℃; for 1h;	100%
In N,N-dimethyl-formamide at 70℃; for 1h;
In N,N-dimethyl-formamide at 80℃; for 4h;	14.5 g

: 1027329-29-8
1-(5-(bromomethyl)-1-methyl-1H-pyrazol-4-yl)ethanone

: 127-08-2
potassium acetate

: 1027329-30-1
(4-acetyl-1-methyl-1H-pyrazol-5-yl)methyl acetate

Conditions

Conditions	Yield
18-crown-6 ether In acetonitrile at 20℃; for 20h;	100%

: 1100212-54-1
5-bromo-7-(bromomethyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazole

: 127-08-2
potassium acetate

: 1100213-62-4
(5-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-7-yl)methyl acetate

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 20 - 40℃; for 1.16667h;	100%

: 1112-67-0
tetrabutyl-ammonium chloride

: 127-08-2
potassium acetate

: 10534-59-5
tetrabutylammonium acetate

Conditions

Conditions	Yield
In methanol	100%
In methanol for 24h; Inert atmosphere;
In methanol for 24h; Inert atmosphere;

: 660417-35-6
2-(1-chloroethyl)-5-(3-chlorophenyl)-1,3,4-oxadiazole

: 127-08-2
potassium acetate

: 1196958-32-3
1-[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]ethyl acetate

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 20℃; for 24h;	100%

: 17455-13-9
18-crown-6 ether

: 127-08-2
potassium acetate

: C2H3O2(1-)*C12H24KO6

Conditions

Conditions	Yield
In water at 20℃; for 12h;	100%

: 127-08-2
potassium acetate

: 52868-15-2
2-bromo-4-chloro-1-phenylbutan-1-one

: C12H13ClO3

Conditions

Conditions	Yield
In acetonitrile	100%

: 1359856-96-4
C12H11Br2FO2

: 127-08-2
potassium acetate

: 1359856-97-5
C14H14BrFO4

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 50℃; for 1h;	100%

: 127-08-2
potassium acetate

: 122996-59-2
1,4-bis(bromomethyl)-2,5-bis-(dodecyloxy)benzene

: 237757-95-8
2,5-bis(acetyl methyl)-1,4-bis(dodecyloxy)benzene

Conditions

Conditions	Yield
With N-butylammonium bromide In chloroform; acetonitrile for 2h; Reflux;	100%
With tetrabutylammomium bromide In chloroform; acetonitrile for 12h; Reflux;	88%