CAS No.67-64-1,Acetone Suppliers,MSDS download

: 67-63-0
isopropyl alcohol

: 67-64-1
acetone

Conditions

Conditions	Yield
With trans-4L1(O)2>ClO4 In acetonitrile at 25℃; for 7h; stoicheiometric oxidation ( electrochemical oxidation in a non-aqueous medium (acetonitrile), an Ag-AgNO3 reference electrode;	100%
With C19H20N3O2Ru(2+)*2F6P(1-) In aq. buffer at 24.84℃; for 1h; pH=1.8; Thermodynamic data; Activation energy; Reagent/catalyst;	100%
With tert-butylethylene; C32H52ClIrP2; sodium t-butanolate at 200℃; for 2h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; Glovebox;	100%

: 110-86-1
pyridine

: 31562-43-3
tert-butylsulfinyl chloride

A: 628-13-7
pyridine hydrochloride

B: 67-64-1
acetone

C: pyridinium tert-butylsulfonate

D: 75-65-0
tert-butyl alcohol

Conditions

Conditions	Yield
With tert.-butylhydroperoxide In chloroform at 20℃; for 2h; Further byproducts given;	A 100% B 20% C 40% D 55%

...Expand

: 76-09-5
2,3-dimethyl-2,3-butane diol

: 67-64-1
acetone

Conditions

Conditions	Yield
With N-Bromosuccinimide; water; potassium carbonate; triphenylbismuthane In acetonitrile for 2h;	100%
With tert.-butylhydroperoxide; bis(acetylacetonato)dioxidomolybdenum(VI) In chlorobenzene at 60℃; for 24h;	99%
With tert.-butylhydroperoxide; chromium tetra(tert-butoxide) In benzene at 20℃; for 24h;	90%

: 3968-30-7
5-cyclopentylidene-2,2-dimethyl-1,3-dioxane-4,6-dione

A: 2873-50-9
butatriene

B: 74-85-1
ethene

C: 124-38-9
carbon dioxide

D: 1165952-91-9
cyclohexa-1,3-diene

E: 67-64-1
acetone

F: 71-43-2
benzene

Conditions

Conditions	Yield
With variation of temp. at 550℃; Product distribution;	A 4% B 11.9% C 100% D 39.2% E 101.9 % F 3.3%

...Expand

: 110-82-7
cyclohexane

: 84210-61-7
perpentene-4 oate de tertiobutyle

A: 92-51-3
cyclohexylcyclohexane

B: 1678-93-9
butylcyclohexane

C: 96009-79-9
cyclohexyl-5 pentanolide-4

D: 67-64-1
acetone

E: 108-29-2
5-methyl-dihydro-furan-2-one

F: 75-65-0
tert-butyl alcohol

Conditions

Conditions	Yield
at 120℃; for 4h; Product distribution; Mechanism; different ratios of reactant, reactants, reaction times and temperatures;	A 5% B 5% C 35% D n/a E 1% F 100%

...Expand

: 110-82-7
cyclohexane

: 80037-90-7
1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindol-2-yloxoyl radical

: 37421-16-2
2-(t-butylazo)prop-2-yl hydroperoxide

A: 89482-40-6
2-cyclohexyloxy-1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindole

B: 93524-81-3
2-tert-butoxy-1,1,3,3-tetramethylisoindoline

C: 67-64-1
acetone

D: 115-11-7
isobutene

Conditions

Conditions	Yield
at 70℃; for 17h; Mechanism; Rate constant; Thermodynamic data; var. of nitroxide, solvent, temp., EA, ΔH(excit.), ΔS(excit.);	A 96% B 82% C 100% D 15%

...Expand

: 83073-73-8
2-(octylsulfonyl)ethyl tert-butyl peroxide

A: 34557-54-5
methane

B: 20466-47-1
2-hydroxyethyl octyl sulfone

C: 67-64-1
acetone

D: 75-65-0
tert-butyl alcohol

Conditions

Conditions	Yield
In various solvent(s) at 145℃; Rate constant; Thermodynamic data; E(act.);	A n/a B 100% C n/a D n/a

...Expand

: 120711-57-1
H-Dmt-Gly-Gly-Ala-OH trifluoroacetate salt

A: 120711-58-2
H-Cys-Gly-Gly-Ala-OH

B: 67-64-1
acetone

Conditions

Conditions	Yield
In ethanol; water Heating;	A 100% B n/a

: 108-22-5
Isopropenyl acetate

: 108-95-2
phenol

A: 67-64-1
acetone

B: 122-79-2
Phenyl acetate

Conditions

Conditions	Yield
With potassium carbonate; Aliquat 336 In neat (no solvent) at 70℃; for 0.5h;	A n/a B 100%
With potassium carbonate; Aliquat 336 In neat (no solvent) at 70℃; for 0.5h; Product distribution;	A n/a B 100%

...Expand

: 34107-52-3
2,2-dimethyl-5-(phenyl-λ3-iodaneylidene)-1,3-dioxane-4,6-dione

A: 2033-24-1
cycl-isopropylidene malonate

B: 591-50-4
iodobenzene

C: 67-64-1
acetone

Conditions

Conditions	Yield
With dirhodium tetraacetate In dichloromethane at 20℃; Product distribution;	A 33% B 100% C 5%

...Expand

: dimethyl(2,2'-bipyridyl)nickel(II)

A: 67552-35-6, 79390-59-3, 79042-98-1
NiCH3(N(CO)2C6H4)(P(C2H5)3)2

B: 14917-14-7
Ni(CO)2(2,2'-bipyridine)

C: 67-64-1
acetone

Conditions

Conditions	Yield
In benzene-d6 40°C, 72 h;	A 100% B n/a C 33%

...Expand

: CpRe(CO)2(COCH3)(CH3)

: 603-35-0
triphenylphosphine

A: (η5-C5H5)Re(CO)2(PPh3)

B: 67-64-1
acetone

Conditions

Conditions	Yield
In 1,4-dioxane; benzene-d6 Kinetics; 100°C (10.25 h);	A 100% B 97%
In benzene-d6 Irradiation (UV/VIS);	A 55% B n/a

...Expand

: 56-23-5
tetrachloromethane

: CpRe(CO)2(COCH3)(CH3)

A: tricarbonylcyclopentadienylrhenium

B: 75-36-5
acetyl chloride

C: 431-03-8
dimethylglyoxal

D: 67-64-1
acetone

Conditions

Conditions	Yield
With CO In dichloromethane-d2 Irradiation (UV/VIS); 355-385 nm; 20 atm CO;;	A 100% B n/a C n/a D n/a

...Expand

: CpRe(CO)2(COCH3)(CH3)

: 4437-51-8
3,4-hexanedione

A: tricarbonylcyclopentadienylrhenium

B: 600-14-6
2,3-Pentanedione

C: 431-03-8
dimethylglyoxal

D: 67-64-1
acetone

Conditions

Conditions	Yield
With CO In benzene-d6 Irradiation (UV/VIS); 355-385 nm;;	A 100% B 68% C 34% D 10%

...Expand

: CpRe(CO)2(CH3)2

A: tricarbonylcyclopentadienylrhenium

B: 431-03-8
dimethylglyoxal

C: 67-64-1
acetone

Conditions

Conditions	Yield
With CO In dichloromethane-d2 Irradiation (UV/VIS); 20 atm CO;;	A 100% B 79% C 5%

...Expand

: CpRe(CO)2(COCH3)(CH3)

A: tricarbonylcyclopentadienylrhenium

B: 431-03-8
dimethylglyoxal

C: 67-64-1
acetone

Conditions

Conditions	Yield
With carbon monoxide In dichloromethane-d2 Irradiation (UV/VIS); Irradiation of complex at 350-380 nm under 20 atm of CO in CD2Cl2 at 6-8°C;;	A 100% B 80% C 8%
With CO In 1,4-dioxane; dichloromethane-d2 Irradiation (UV/VIS); ca. 20 atm CO; 355-385 nm light, 22 min.;	A 100% B 78% C 6%

...Expand

: (3-(tert-butylperoxy)pentane-3yl)benzene

A: 93-55-0
1-phenyl-propan-1-one

B: 67-64-1
acetone

C: 75-65-0
tert-butyl alcohol

Conditions

Conditions	Yield
With air In [D3]acetonitrile at 22℃; for 1h; UV-irradiation; Inert atmosphere;	A 100% B 41.9% C 25.9%

...Expand

: 1118-66-7
4-amino-3-penten-2-one

: 67-64-1
acetone

Conditions

Conditions	Yield
at 250℃; for 0.666667h; Heating; Inert atmosphere;	99.76%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

A: 123-56-8
Succinimide

B: 67-64-1
acetone

Conditions

Conditions	Yield
With N-iodo-succinimide In benzene for 0.916667h; Product distribution; Mechanism; Irradiation; varying reaction time;	A 88% B 99%

: 98-86-2
acetophenone

: 67-63-0
isopropyl alcohol

A: 1445-91-6
(S)-1-phenylethanol

B: 67-64-1
acetone

Conditions

Conditions	Yield
With cis-[Ru(PPh2)(CH2)5PPh2(ampi)Cl2]; potassium hydroxide at 80℃; for 0.5h; Reagent/catalyst; Concentration; Schlenk technique;	A 99% B n/a
Stage #1: isopropyl alcohol With dichloro(1,5-cyclooctadiene)ruthenium(II); (R)-(6-methoxyquinolin-4-yl)((1S,2R,4S,5R)-5-vinylquinuclidin-2-yl)methanamine at 20℃; for 0.5h; Inert atmosphere; Stage #2: With potassium hydroxide for 0.5h; Inert atmosphere; Stage #3: acetophenone at 0℃; for 96h; Inert atmosphere; enantioselective reaction;	A 83% B n/a
With potassium hydroxide; oxalyl (1R,2R)-N,N'-bis[2-(amino)cyclohexyl]diamide; tris(triphenylphosphine)ruthenium(II) chloride at 20℃; for 24h; Product distribution; Further Variations:; Reagents;

...Expand

: 486-25-9
9-fluorenone

: 67-63-0
isopropyl alcohol

A: 1689-64-1
9-Fluorenol

B: 67-64-1
acetone

Conditions

Conditions	Yield
With [RuCl2(triphenylphosphine)((6-((3,5-dimethyl-pyrazol-1-yl)pyridin-2-yl)methylene)-p-tolyl-amine)]*0.5Et2O; potassium isopropoxide at 82℃; under 750.075 Torr; for 5.16667h; Inert atmosphere;	A 99% B n/a
With sodium hydroxide; RuCl2(PPh3)(iBu-BTP) at 82℃; under 750.075 Torr; for 9h;	A 97 % Chromat. B n/a

...Expand

: (H2O)5CrC(CH3)2OH(2+)

A: chromium (III) ion

B: 67-64-1
acetone

Conditions

Conditions	Yield
With Fe(3+) In water; isopropyl alcohol Kinetics; byproducts: H(1+); excess of Fe(3+) in 1 M aq. i-PrOH at 24.8°C under N2 by controlled ionic strength;	A n/a B 99%

: ethyl 2-benzoyl-6-methylhept-5-enoate

A: ethyl 2-phenylcyclopent-2-ene-1-carboxylate

B: 67-64-1
acetone

Conditions

Conditions	Yield
With gold(III) chloride In 1,2-dichloro-ethane at 25℃; Reagent/catalyst; Solvent; Sealed tube;	A 99% B n/a
With N-iodo-succinimide In 1,2-dichloro-ethane at 20℃; for 24h; Reagent/catalyst;	A 66% B n/a

: 4-fluoro-2-(5-methylhex-4-en-1-yl)benzaldehyde

A: 3-fluoro-6,7-dihydro-5H-benzo[7]annulene

B: 67-64-1
acetone

Conditions

Conditions	Yield
With gold(III) chloride In 1,2-dichloro-ethane at 25℃; Sealed tube;	A 99% B n/a

: 80-15-9
Cumene hydroperoxide

A: 67-64-1
acetone

B: 108-95-2
phenol

Conditions

Conditions	Yield
With iron(III) perchlorate In acetonitrile Product distribution; var. act.: CuClO4; var. solv.: CH2Cl2, toluene; var. conc.; determination of half life;	A 98.9% B 96.3%
With N-Phenyl-2-naphthylamine; cobalt(II) phthalocyanine In decalin at 40℃; Rate constant; Kinetics; var. temperatures, var. catalysts, var. solvents, without NA;
In chlorobenzene at 75℃; Kinetics; various phosphites;

: 67-63-0
isopropyl alcohol

A: 187737-37-7
propene

B: 67-64-1
acetone

Conditions

Conditions	Yield
6xSAlH (sulfated alumina) at 246.85℃; Product distribution; Further Variations:; Catalysts; atmospheric pressure;	A 98.4% B 1.6%
bismuth molybdate; bismuth molybdate at 190℃; Product distribution; with Bi2Mo2O9 (β-phase) catalyst;	A 12% B 88%
With cobalt ferrite; oxygen at 299.84℃; for 3h; Autoclave;	A 52% B 40%

: 75-91-2
tert.-butylhydroperoxide

: 30931-67-0
2,2'-azinobis-(3-ethyl-2,3-dihydrobenzothiazole-6-sulphonate) diammonium salt

A: 67-56-1
methanol

B: 50-00-0
formaldehyd

C: C18H18N4O6S4(1+)*2H3N

D: 67-64-1
acetone

E: 75-65-0
tert-butyl alcohol

Conditions

Conditions	Yield
Fe(III)T4MPyP In water at 30℃; Rate constant; Kinetics; Mechanism; the catalyst Fe(III)T4MPyP is 5,10,15,20-tetra(N-methyl-4-pyridyl)-porphyrinatoiron(III) pentachloride; pH 9.2; investigation of the dependence of velocity constant on ionic strength, pH and t-butyl hydroperoxide concentration;	A 3% B n/a C 72% D 4% E 98%

...Expand

: 87051-12-5
(4aRS,7aRS)-4a,7a-dihydro-3,3-dimethyl-6,7a-diphenyl-7H-cyclopenta<1,2-e><1,2,4>trioxine

: 114390-60-2
(1RS,2RS)-1,4-diphenylcyclopent-3-en-1,2 diol

B: 67-64-1
acetone

Conditions

Conditions	Yield
With acetic acid; zinc at 16℃; for 0.333333h;	A 98% B n/a

: 99-91-2
para-chloroacetophenone

: 67-63-0
isopropyl alcohol

A: 3391-10-4
1-(p-chlorophenyl)ethyl alcohol

B: 67-64-1
acetone

Conditions

Conditions	Yield
With C58H49ClN5P2Ru(1+)*Cl(1-); potassium isopropoxide at 82℃; for 0.00555556h; Inert atmosphere;	A 98% B n/a
With sodium hydroxide; RuCl2(PPh3)(iBu-BTP) at 82℃; under 750.075 Torr; for 30h;	A 89 % Chromat. B n/a
With [RuCl2(triphenylphosphine)((6-((3,5-dimethyl-pyrazol-1-yl)pyridin-2-yl)methylene)-p-tolyl-amine)]*0.5Et2O; potassium isopropoxide at 82℃; under 750.075 Torr; for 1.16667h; Inert atmosphere;	A 98 %Chromat. B n/a

...Expand

: NiMe2(PEt3)2

A: 16787-33-0
(CO)2Ni(P(C2H5)3)2

B: 75-07-0
acetaldehyde

C: 431-03-8
dimethylglyoxal

D: 67-64-1
acetone

Conditions

Conditions	Yield
With carbon monoxide In diethyl ether Et2O soln. of Ni complex stirred under CO at -78°C for 0.2 h, warmed to room temp.; drying up; GLC anal.;	A n/a B 0% C 0% D 98%

...Expand

: 96-09-3
styrene oxide

: 67-64-1
acetone

: 52129-03-0
2,2-dimethyl-4-phenyl-1,3-dioxolane

Conditions

Conditions	Yield
With FeOx-pillared bentonite at 30℃; for 0.0833333h; Reagent/catalyst; Time; Temperature; Solvent;	100%
erbium(III) triflate at 20℃; for 0.5h;	99%
With trichloro(trifluoromethanesulfonato)titanium(IV); n-tetrabutylammonium hydroxide In water for 0.166667h; Ambient temperature;	98%

: 120-57-0
piperonal

: 67-64-1
acetone

: 108439-88-9
(1E,4E)-1,5-bis(benzo[d][1,3]dioxol-5-yl)penta-1,4-dien-3-one

Conditions

Conditions	Yield
With sodium hydroxide In ethanol for 0.00833333h; Irradiation;	100%
With sodium hydroxide In ethanol; water at 20℃;	85%
With sodium hydroxide In ethanol; water at 20℃; Aldol Addition;	79%

: 555-16-8
4-nitrobenzaldehdye

: 67-64-1
acetone

: 88958-64-9, 88958-65-0, 97600-21-0, 57548-40-0
1-(4-nitrophenyl)-1-hydroxy-3-butanone

Conditions

Conditions	Yield
With Zn(2+)-(TyrOEt)2 In water at 40℃; for 24h; pH 7;	100%
With sodium hydroxide at 25℃; for 0.166667h;	100%
With Fe(OH)3/Fe3O4 at 50℃; for 3h;	99%

: 2004-06-0
6-Chloropurine riboside

: 67-64-1
acetone

: 39824-26-5
6-chloro-9-(2,3-O-isopropylidene-β-D-ribofuranosyl)-9H-purine

Conditions

Conditions	Yield
With toluene-4-sulfonic acid at 20℃; for 3h;	100%
In perchloric acid for 3h; Ambient temperature;	94%
With perchloric acid at 25℃;	94%

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

: 67-64-1
acetone

: 2175-91-9
6,6'-dimethyl fulvene

Conditions

Conditions	Yield
Stage #1: cyclopenta-1,3-diene; acetone With pyrrolidine In methanol at 20℃; Inert atmosphere; Stage #2: With acetic acid In methanol for 0.15h;	100%
With pyrrolidine In methanol at -10 - 20℃; for 1h; Inert atmosphere;	100%
With methylamine for 4.5h;	92%

: 123-08-0
4-hydroxy-benzaldehyde

: 67-64-1
acetone

: 3654-49-7
(1E,4E)-1,5-bis(4-hydroxyphenyl)penta-1,4-dien-3-one

Conditions

Conditions	Yield
With hydrogenchloride In tetrahydrofuran for 264h;	100%
With hydrogenchloride; acetic acid at 25 - 30℃; for 2h; Heating;	95%
With hydrogenchloride In acetic acid at 25 - 30℃; for 2h;	95%

: 123-11-5
4-methoxy-benzaldehyde

: 67-64-1
acetone

: 943-88-4
4-(p-methoxyphenyl)-3-butene-2-one

Conditions

Conditions	Yield
With sodium hydroxide In water at 120℃; under 6750.68 Torr; Aldol condensation; Continuous flow;	100%
With 1-n-butyl-3-methylimidazolim bromide; bovine serum albumin at 60℃; for 6h; Aldol Condensation; Green chemistry; Enzymatic reaction;	98%
With sodium hydroxide for 72h; Ambient temperature;	97%

: 630-19-3
pivalaldehyde

: 67-64-1
acetone

: 101713-95-5
4-hydroxy-2,2-dimethyl-6-heptanone

Conditions

Conditions	Yield
With sodium hydroxide at 20℃;	100%
Stage #1: acetone With sodium hydroxide In water at 20℃; Microfluidic conditions; Stage #2: pivalaldehyde; acetone In water at 20℃; Microfluidic conditions;	100%
With n-butyllithium; diisopropylamine In tetrahydrofuran at -78℃; for 0.583333h;	47%

: 1068-57-1
acetic acid hydrazide

: 67-64-1
acetone

: 3742-63-0
acetic acid isopropylidenehydrazide

Conditions

Conditions	Yield
In cyclohexane at 55℃; for 16h;	100%
In hexane Reflux;	93%
In hexane for 4h; Heating;	91%

: 66-99-9
β-naphthaldehyde

: 67-64-1
acetone

: 75032-63-2
4-(2-naphtalenyl)-3-buten-2-one

Conditions

Conditions	Yield
With potassium hydroxide In methanol; water at 20℃; for 0.5h;	100%
With boehmite at 55℃; for 24h; Aldol Condensation; Green chemistry;	55%
With sodium hydroxide

: 93-02-7
2,5-dimethoxybenzaldehyde

: 67-64-1
acetone

: 118709-30-1
trans-1-(2,5-dimethoxyphenyl)-2-buten-3-one

Conditions

Conditions	Yield
With sodium hydroxide at 23℃; for 6.5h;	100%
Stage #1: 2,5-dimethoxybenzaldehyde; acetone With L-proline In dimethyl sulfoxide at 20℃; for 48h; Stage #2: With hydrogenchloride In water; dimethyl sulfoxide for 3h;	62.5%
With sodium hydroxide at 20℃; for 0.5h;	53%

: 536-74-3
phenylacetylene

: 67-64-1
acetone

: 1719-19-3
2-Methyl-4-phenyl-3-butyn-2-ol

Conditions

Conditions	Yield
phosphazene base-P4-tert-butyl In hexane; dimethyl sulfoxide at 120℃; for 24h;	100%
Stage #1: phenylacetylene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Inert atmosphere; Stage #2: acetone In tetrahydrofuran; hexane at -78 - 20℃;	100%
With Nd(3+)8Na(1+)10C4H9O(1-)*HO(1-) In dimethyl sulfoxide at 30℃; for 24h; Catalytic behavior; Concentration; Solvent; Reagent/catalyst; Inert atmosphere;	100%

: 62-53-3
aniline

: 67-64-1
acetone

: 1124-52-3
N-(propan-2-ylidene)aniline

Conditions

Conditions	Yield
With cis-(Cl,Cl)-[Re(p-NC6H4CH3)Cl2(py-2-COO)(PPh3)] at 70℃; for 24h; Inert atmosphere;	100%
With microporous zeolite at 230℃; for 24h; Sealed tube; Autoclave;	97%
sodium hydrogen sulfate; silica gel at 50 - 52℃; for 0.0333333h; microwave irradiation;	75%

: 137-07-5
2-amino-benzenethiol

: 67-64-1
acetone

: 25111-89-1
2,2-dimethyl-2,3-dihydro-benzothiazole

Conditions

Conditions	Yield
at 0℃; for 2h; gas/solid reaction;	100%
Stage #1: 2-amino-benzenethiol; acetone In neat (no solvent) at 50℃; for 1h; Green chemistry; Stage #2: With o-benzenedisulfonimide In neat (no solvent) at 50℃; for 48h; Green chemistry;	87%
With aluminum oxide at 20℃; for 0.5h;	84%

: 100-10-7
4-dimethylamino-benzaldehyde

: 67-64-1
acetone

: 5432-53-1
4-p-dimethylaminophenyl-3-buten-2-one

Conditions

Conditions	Yield
With sodium hydroxide for 72h; Ambient temperature;	100%
With water; potassium hydroxide at 20℃; for 0.2h;	82%
With sodium hydroxide In water at 0 - 20℃; Aldol condensation;	67.73%

: 109-80-8
1.3-propanedithiol

: 67-64-1
acetone

: 6007-22-3
2,2-dimethyl-1,3-dithiane

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In dichloromethane at 25℃;	100%
With titanium tetrachloride	79%
acid	78%

: 57-55-6
propylene glycol

: 67-64-1
acetone

: 1193-11-9, 116944-25-3
2,2,4-trimethyl-1,3-dioxolane

Conditions

Conditions	Yield
With cyclohexane at 105℃; for 1h; Dean-Stark;	100%
With Amberlyst 36 at 50℃; for 2h;	75%
With 4 A molecular sieve; Amberlyst A 15 In tetrahydrofuran for 24h; Ambient temperature;	35%

: 5973-71-7
3,4-dimethylbenzaldehyde

: 67-64-1
acetone

: 97241-86-6
(E)-4-(3,4-dimethylphenyl)but-3-en-2-one

Conditions

Conditions	Yield
With sodium hydroxide In water at 0 - 25℃; for 6h;	100%
With sodium hydroxide
With sodium hydroxide In water at 25℃; for 12h;

: 5906-99-0
2-nitrobenzenesulfonyl hydrazide

: 67-64-1
acetone

: 6655-27-2
N-isopropylidene-N’-2-nitrobenzenesulfonyl hydrazine

Conditions

Conditions	Yield
at 0℃; for 1h;	100%
at 24℃; for 0.166667h; Inert atmosphere;	95%
at 0 - 23℃;	89%

: 67-64-1
acetone

: 56-81-5
glycerol

: 100-79-8
(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol

Conditions

Conditions	Yield
With sulfuric acid at 40℃; Reagent/catalyst;	100%
With toluene-4-sulfonic acid In hexane at 70℃; for 12h; Dean-Stark; Molecular sieve; Inert atmosphere;	100%
Acidic conditions;	100%

: 67-64-1
acetone

: 6287-38-3
3,4-dichlorobenzaldehyde

: 30983-80-3
(1E,4E)-1,5-bis(3,4-dichlorophenyl)penta-1,4-dien-3-one

Conditions

Conditions	Yield
With sodium hydroxide In ethanol; water at 20℃; for 1h;	100%
With sodium hydroxide In ethanol; water at 20℃; Aldol Addition;	70%
With sodium hydroxide
With sodium hydroxide In ethanol

: 67-64-1
acetone

: 58-96-8
uridine

: 362-43-6
2',3'-O-isopropylideneuridine

Conditions

Conditions	Yield
With sulfuric acid at 20℃; for 1h;	100%
Stage #1: acetone; uridine With sulfuric acid at 20℃; for 1h; Stage #2: With triethylamine In acetone Product distribution / selectivity;	100%
With sulfuric acid at 20℃; for 1h;	100%

: 67-64-1
acetone

: 4114-31-2
ethylhydrazine carboxylate

: 6637-60-1
N'-isopropylidenehydrazinecarboxylic acid ethyl ester

Conditions

Conditions	Yield
	100%
With magnesium sulfate Reflux;	100%
for 2h; Heating;	98%

: 67-64-1
acetone

: 19214-95-0
(2-2H)propan-2-(2H)ol

Conditions

Conditions	Yield
With lithium aluminium deuteride In diethylene glycol dimethyl ether at 0℃; for 1h; Inert atmosphere;	100%
With pyrographite; platinum; deuterium at 25℃; under 1520 Torr; an mit Eisensalz;
With lithium aluminium deuteride

: 67-64-1
acetone

: 6868-83-3
acetylmethanenitrolic acid

Conditions

Conditions	Yield
With dinitrogen tetraoxide In tetrachloromethane 1.) 0 deg C, 20 min, 2.) 20 deg C, 40 min;	100%
With nitric acid

: 67-64-1
acetone

: 67-63-0
isopropyl alcohol

Conditions

Conditions	Yield
With hydrogen; mer-Os(PPh3)3HBr(CO) In toluene at 150℃; under 51680 Torr; for 3h;	100%
With hydrogen; sodium methylate; chromium(0) hexacarbonyl In methanol at 120℃; under 75006 Torr; for 3h;	100%
With hydrogen; Ru((R,R)-cyP2N2)HCl In benzene-d6 at 20℃; under 2280.15 Torr; for 12h; Product distribution / selectivity; Alkaline conditions; Cooling with liquid nitrogen;	100%

: 67-64-1
acetone

: 18449-76-8
methyl α-D-lyxopyranoside

: 60562-98-3
methyl 2,3-O-isopropylidene-α-D-lyxopyranoside

Conditions

Conditions	Yield
With 4 A molecular sieve; amberlyst-15 (H form) at 23℃; for 4h;	100%
With sulfuric acid; copper(II) sulfate for 24h; Ambient temperature;	81%
With sulfuric acid
With phosphorus pentoxide

: 67-64-1
acetone

: 58-61-7
adenosine

: 362-75-4
2',3'-isopropylidene adenosine

Conditions

Conditions	Yield
With toluene-4-sulfonic acid; orthoformic acid triethyl ester at 20℃;	100%
With p-toluenesulfonic acid monohydrate for 3h; Inert atmosphere;	100%
With toluene-4-sulfonic acid at 20℃; for 1h; Inert atmosphere;	99%

: 100-52-7
benzaldehyde

: 67-64-1
acetone

: 5381-93-1, 86734-67-0, 86734-69-2, 127707-68-0
1-hydroxy-1-phenyl-3-butanone

Conditions

Conditions	Yield
With sodium hydroxide at 20℃;	100%
Stage #1: acetone With sodium hydroxide In water at 20℃; Microfluidic conditions; Stage #2: benzaldehyde; acetone In water at 20℃; Microfluidic conditions;	100%
With pyrrolidine; 4-nitro-phenol at 20℃; for 2.5h;	99.4%

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