Conditions | Yield |
---|---|
With acetic acid; dimethyl amine at 170 - 180℃; under 52505.3 Torr; for 0.00277778h; Flow reactor; | 98.1% |
With secondary amine salt In water at 15 - 44℃; for 1h; | 96.6% |
With L-proline In water at 42.84℃; for 0.5h; Kinetics; Mechanism; Reagent/catalyst; Temperature; Green chemistry; | 91.1% |
Conditions | Yield |
---|---|
With aluminum oxide; pyridinium chlorochromate In hexane for 0.2h; Ambient temperature; | 98% |
With manganese(IV) oxide In diethyl ether Oxidation; | 76% |
at 500℃; beim Leiten ueber Messing; |
Conditions | Yield |
---|---|
With thexylbromoborane dimethyl sulfide complex In carbon disulfide; dichloromethane at -20 - 20℃; for 1h; | 94% |
Conditions | Yield |
---|---|
With oxygen In water at 350℃; under 750.075 Torr; | 91.1% |
With air; cobalt molybdenum at 319.9 - 379.9℃; Rate constant; Product distribution; | 88.1% |
With silicsa-alumina supported Mo12Bi1.7Fe2.0Co6.75Ni1.0Cs0.2Ox In water at 345℃; for 200h; Temperature; Inert atmosphere; | 81.07% |
Conditions | Yield |
---|---|
With water; iodine In 1,4-dioxane for 24h; Reflux; | 91% |
Conditions | Yield |
---|---|
With oxygen; Bi-Mo oxide (1/1) at 400℃; Rate constant; Kinetics; also without O2; other temperature; | 90% |
With oxygen; Mo-Bi-Fe-Co-Ni-K based mixed metal oxide In water at 340 - 360℃; under 760.051 Torr; for 100h; | 89.9% |
With Mo12Bi0.5Fe2.4Co7.2Zn1.1Sb0.7Si7W0.3K0.5O(x); water; oxygen at 340℃; for 0.001h; Sealed tube; Inert atmosphere; | 88.8% |
Conditions | Yield |
---|---|
With nitrogen; Mo12Co5.7Fe3.8Bi0.5Ce0.1Tl0.3Sb0.5O49.1; water; oxygen at 380℃; for 10005h; Reagent/catalyst; | A 65% B 89% |
isobutene
A
2-methylpropenal
B
carbon dioxide
C
carbon monoxide
Conditions | Yield |
---|---|
With air; pelleted Fe-Te-Mo-O at 430℃; Yields of byproduct given; | A 83.8% B n/a C n/a |
With air; pelleted Fe-Te-Mo-O at 430℃; Product distribution; further temperatures: 370, 400 deg C; effect of various catalyst supports investigated; | A 83.8% B n/a C n/a |
With oxygen multicomponent oxide catalyst(Co, Mo, Bi, Sb, Fe, K); |
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; palladium diacetate; trifluoroacetic acid; 3-amino propanoic acid In acetonitrile at 60℃; for 24h; Sealed tube; | 82% |
With oxygen; C4H8N3O2Pb(1+)*CF3O3S(1-) In various solvent(s) under 760 Torr; Ambient temperature; Yield given; | |
at 400℃; Dehydrierung an einem Cu-Cr-Zn-Cd-Oxydkatalysator; |
tert-butyl alcohol
A
2-methylpropenal
B
poly(methacrylic acid)
C
isobutene
Conditions | Yield |
---|---|
With oxygen; silica-alumina In water at 355℃; Product distribution / selectivity; | A 78.4% B 1.9% C 1.1% |
With oxygen; silica-alumina In water at 355℃; Product distribution / selectivity; | A 78.1% B 2.2% C 1% |
With oxygen; 5% Pd/zirconia In water at 130℃; under 36003.6 Torr; Product distribution / selectivity; autoclave; | |
With oxygen; palladium on silica gel In water at 130℃; under 36003.6 Torr; Product distribution / selectivity; autoclave; |
isobutene
A
2-methylpropenal
B
ethanol
C
acetone
D
acetonitrile
E
propiononitrile
F
methacrylonitrile
Conditions | Yield |
---|---|
With nitrogen(II) oxide; nickel(II) oxide; aluminum oxide at 410℃; Product distribution; var. cat.: pure NiO, NiO supported by alumina, silica, magnesia, alumina-magnesia, silica-alumina, silica-magnesia; var. temp.; | A 4.5% B 2% C 2.5% D 7.5% E 2% F 76% |
isobutene
A
2-methylpropenal
B
acetone
C
acetonitrile
D
methacrylonitrile
Conditions | Yield |
---|---|
With nitrogen(II) oxide; nickel(II) oxide; aluminum oxide at 410℃; var. cat. and temp.; | A 4.5% B 2.5% C 7.5% D 76% |
isobutene
A
2-methylpropenal
B
poly(methacrylic acid)
C
acetic acid
Conditions | Yield |
---|---|
With air; water; CoMoTeO at 425℃; | A 68.2% B 9% C 1% |
With air; V-Mo-Te-O at 405℃; | A 59% B 6% C 3% |
With air; water; CoMoTeO at 375℃; Product distribution; Thermodynamic data; direct catalytic oxidation; varying: temperatures: 300 to 450 deg C; reactant composition; | A 27.5% B 39.5% C 4% |
Conditions | Yield |
---|---|
With air; iron-tellurium-molybdenum-oxide at 419.85℃; for 0.000916667h; Product distribution; Further Variations:; Temperatures; Catalysts; time of contact; Oxidation; | A 64.8% B n/a |
Conditions | Yield |
---|---|
With oxygen; ozone In gas Product distribution; gas-phase ozonolysis of alkenes; formation of OH radicals; use of CO as scavenger for OH radicals; | A 54% B 28% C 21% |
formaldehyd
propionaldehyde
A
2-methylpropenal
B
2-methyl-2-pentenal
Conditions | Yield |
---|---|
With aniline hydrochloride In N,N-dimethyl acetamide at 125℃; for 3h; Autoclave; | A 30% B 17% |
Conditions | Yield |
---|---|
With phosphoric acid; oxygen; 4-methoxy-phenol; palladium 10% on activated carbon In tert-butyl alcohol at 90℃; under 2250.23 - 30003 Torr; for 2h; Product distribution / selectivity; Heating / reflux; | A 24.6% B 9.2% |
With oxygen; 4-methoxy-phenol; palladium 10% on activated carbon In tert-butyl alcohol at 90℃; under 2250.23 - 30003 Torr; for 2h; Product distribution / selectivity; Heating / reflux; | A 10.8% B 3.3% |
With nitrogen; water; Mo12Bi1Fe1.5Co8Zn0.2Cs0.4Sb0.8Ox on graphite at 325 - 340℃; Conversion of starting material; Industry scale; Continuous process; |
Conditions | Yield |
---|---|
With air; dihydrogen peroxide for 0.5h; Product distribution; Kinetics; Further Variations:; Reagents; Oxidation; UV-irradiation; | A 2.8% B 19.1% C 20.5% D 3.7% |
Conditions | Yield |
---|---|
With oxygen; Mo1.0V0.3Nb0.1On at 350℃; under 760.051 Torr; Product distribution / selectivity; Gas phase; | A 0.2% B 18% |
With oxygen; Mo1.0V0.3Sb0.7Nb0.1On at 430℃; under 760.051 Torr; Product distribution / selectivity; Gas phase; | A 2.3% B 0.1% |
With oxygen; Mo1.0V0.3Te0.16Nb0.1On at 430℃; under 760.051 Torr; Product distribution / selectivity; Gas phase; | A 1.4% B 0.1% |
Conditions | Yield |
---|---|
With oxygen; Mo1.0Sb0.5Ce0.09Sn0005Ag0001On at 525℃; under 760.051 Torr; Product distribution / selectivity; Gas phase; | A 11.5% B 0.3% C 4.2% |
With oxygen; Mo1.0Sb0.5Ce0.09Ag0003On at 500℃; under 760.051 Torr; Product distribution / selectivity; Gas phase; | A 9.8% B 0.5% C 1.2% |
With oxygen; Mo1.0Sb0.5Ce0.1On at 500℃; under 760.051 Torr; Product distribution / selectivity; Gas phase; | A 8.9% B 0.3% C 0.9% |
With oxygen; Mo1.0Sb0.5Bi0.1Sn0.01On at 500℃; under 760.051 Torr; Product distribution / selectivity; Gas phase; | A 8.2% B 0.3% C 5.1% |
With oxygen; MoV0.3Te0.23P0.3 at 400℃; Product distribution; Further Variations:; Temperatures; Catalysts; | A 3.4 % Chromat. B 3.6 % Chromat. C 6.4 % Chromat. |
Conditions | Yield |
---|---|
With oxygen; Mo1.0V0.3Te0.16Nb0.2On at 390℃; under 760.051 Torr; Product distribution / selectivity; Gas phase; | A 1.9% B 0.4% C 1.8% |
With oxygen; 2.5Cs(1+)*0.34H(1+)*0.08Ni(2+)*PMo12O40(3-)=Cs2.5H0.34Ni0.08PMo12O40 at 340℃; Product distribution; var. conc. of Cs in catalyst, effect of var. transition metals; | |
With Mo12O40P; oxygen at 623℃; other catalysts; | |
With Mo11O40PV(4-)*2.5H4N(1+)*H(1+)*0.5Cs(1+); oxygen at 340℃; under 760.051 Torr; for 18h; |
Conditions | Yield |
---|---|
With oxygen; bis(ethylene)rhodium acetylacetonate In toluene at 80℃; under 37503 Torr; for 1h; | A 1% B 1.3% |
With oxygen; bis(ethylene)rhodium acetylacetonate In toluene at 80℃; under 37503 Torr; for 1h; | A 1% B 1.3% |
With ozone at 24.9℃; under 760 Torr; Rate constant; Thermodynamic data; other temperatures (240-324 K), Arrhenius parameters; | A 35 % Chromat. B 18 % Chromat. |
With dinitrogen pentoxide at 296℃; under 740 Torr; Mechanism; mechanism of the reaction with NO3 radical; |
dihydro-4-methylfuran-2,3-dione
2-methylpropenal
Conditions | Yield |
---|---|
at 300℃; Erhitzen im Stickstoff-Strom; | |
at 280 - 300℃; |
Conditions | Yield |
---|---|
at 450℃; |
2-methylpropane-1,2,3-triol
2-methylpropenal
Conditions | Yield |
---|---|
With sulfuric acid | |
With sulfuric acid |
1,1-diethoxy-2-methyl-2-propene
2-methylpropenal
Conditions | Yield |
---|---|
With sulfuric acid | |
With tartaric acid | |
With sulfuric acid |
3-chloro-2-methylpropenol
2-methylpropenal
Conditions | Yield |
---|---|
With sulfuric acid; isobutyric Acid | |
With sulfuric acid |
2-methyl-2-propene-1-al oxime
2-methylpropenal
Conditions | Yield |
---|---|
With acetic acid; sodium nitrite at 60 - 70℃; |
2-methylpropenal
methyl 2-methoxy-6-hydroxy-7,8-dihydro-5-quinolinecarboxylate
(+/-)-7,8,9,10-tetrahydro-8-hydroxy-2-methoxy-7-methyl-11-oxo-5,9-methanocycloocta[b]pyridine-5(6H)-carboxylic acid methyl ester
Conditions | Yield |
---|---|
With quinindine for 43h; | 100% |
N,N,N',N'-tetramethylguanidine In dichloromethane Ambient temperature; | 93% |
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; chloro-trimethyl-silane; lithium iodide In various solvent(s) at -78℃; for 1h; | 100% |
2-methylpropenal
n-pentylcopper
2-methyl-1-octanal
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; chloro-trimethyl-silane; lithium iodide In various solvent(s) at -78℃; for 0.1h; | 100% |
2-methylpropenal
4-(2-(S)-methoxymethyl-pyrrolidin-1-yl)-3-(tert-butyldimethylsiloxy)-1,3-butadiene
Conditions | Yield |
---|---|
In toluene Diels-Alder reaction; a) -20 deg C, 30 min, b) RT, 22 h; | 100% |
2-methylpropenal
Conditions | Yield |
---|---|
In toluene Diels-Alder reaction; a) -20 deg C, 30 min, b) RT, 22 h; | 100% |
2-methylpropenal
bis(2-pyridyldimethylsilyl)methane
(E,E)-2-pyridyldimethyl(3-methylbuta-1,3-dienyl)silane
Conditions | Yield |
---|---|
Stage #1: bis(2-pyridyldimethylsilyl)methane With n-butyllithium In diethyl ether; hexane at -78℃; Metallation; Stage #2: 2-methylpropenal In diethyl ether; hexane at -78 - 20℃; Peterson-type olefination; Further stages.; | 100% |
Stage #1: bis(2-pyridyldimethylsilyl)methane With n-butyllithium In diethyl ether; hexane at -78℃; for 1h; Stage #2: 2-methylpropenal In diethyl ether; hexane at -78 - 20℃; for 1.5h; Peterson-type olefination; |
2-methylpropenal
(1R,4aR,8aS)-1,4a-Dimethyl-5-vinyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester
(1R,4aR,10aS)-8-Formyl-1,4a,8-trimethyl-1,2,3,4,4a,6,7,8,8a,9,10,10a-dodecahydro-phenanthrene-1-carboxylic acid methyl ester
Conditions | Yield |
---|---|
at 25℃; for 8h; Diels-Alder cycloaddition; | 100% |
at 25℃; for 8h; Cycloaddition; Diels-Alder reaction; | 100% |
at 25℃; for 8h; Diels-Alder Reaction; Neat (no solvent); | 100% |
2-methylpropenal
N-benzyl-N-[(1S,6R)-6-formyl-6-methyl-2-cyclohexen-1-yl]carbamic acid methyl ester
Conditions | Yield |
---|---|
With 4 A molecular sieve; TBDMS-substituted (1R,2R)-salen-Co(III)-SbF6 In dichloromethane at 20℃; for 20h; Diels-Alder cycloaddition; | 100% |
2-methylpropenal
5-(4-methoxyphenyl)-2-phenyl-2H-tetrazole
Conditions | Yield |
---|---|
In benzene for 2h; UV-irradiation; | 100% |
Conditions | Yield |
---|---|
Stage #1: (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at 0℃; Stage #2: 2-methylpropenal In tetrahydrofuran; hexane at -78℃; Further stages.; | 100% |
Conditions | Yield |
---|---|
With 10H-phenothiazine; hydroquinone at 40℃; for 22h; Reagent/catalyst; Concentration; Inert atmosphere; | 99% |
With 1.5 % Au/alumina; oxygen at 60℃; under 9034.64 Torr; Catalytic behavior; chemoselective reaction; | 99.7% |
With oxygen at 69.84℃; under 1500.15 Torr; for 2h; Reagent/catalyst; Autoclave; | 98% |
2-methylpropenal
Conditions | Yield |
---|---|
Stage #1: 2-methylpropenal; triisopropylsilyl (E)-propylideneazinate With trifluorormethanesulfonic acid; (S)-3,3-diphenyl-1-(o-tolyl)hexahydropyrrolo[1,2-c]-[1,3,2]oxazaborole In dichloromethane; toluene at -60℃; for 12h; Inert atmosphere; Schlenk technique; Stage #2: With sodium tetrahydroborate In methanol; dichloromethane; toluene at -60 - 20℃; Catalytic behavior; Reagent/catalyst; Solvent; enantioselective reaction; | 99.7% |
2-methylpropenal
cyclopenta-1,3-diene
endo-bicyclo[2.2.1]hept-5-ene-2-methyl-2-carboxaldehyde
Conditions | Yield |
---|---|
With C30H29B2Br6N2O6P In dichloromethane at -78℃; for 1h; Reagent/catalyst; Diels-Alder Cycloaddition; Schlenk technique; Inert atmosphere; Molecular sieve; enantioselective reaction; | 99% |
With [BCl2(1-methylimidazole)][Al2Cl7] In neat (no solvent) at 0℃; for 0.0833333h; Diels-Alder Cycloaddition; Inert atmosphere; | 91% |
In benzene at 20℃; | |
In benzene at 80℃; | |
With C35H56AlNO2S In chloroform-d1 at 20℃; for 1.5h; Reagent/catalyst; Diels-Alder Cycloaddition; Inert atmosphere; diastereoselective reaction; | 27 %Spectr. |
2-methylpropenal
2-methyl-2-(trimethylsilyloxy)-3-pentanone
(4R*,5R*)-5-hydroxy-2,4,6-trimethyl-2-<(trimethylsilyl)oxy>-6-hepten-3-one
Conditions | Yield |
---|---|
Stage #1: 2-methyl-2-(trimethylsilyloxy)-3-pentanone With lithium diisopropyl amide In tetrahydrofuran; hexane at -78℃; Inert atmosphere; Stage #2: 2-methylpropenal In tetrahydrofuran; hexane at -78℃; for 0.25h; Inert atmosphere; | 99% |
With lithium diisopropyl amide 1.) THF, hexane, -78 deg C, 25 min, 2.) from -78 deg C to RT; Yield given. Multistep reaction; |
2-methylpropenal
cyclopenta-1,3-diene
(2R)-2-methylbicyclo[2.2.1]hept-5-ene-2-carbaldehyde
Conditions | Yield |
---|---|
With (R)-3,3'-bis(2-hydroxyphenyl)-2,2'-dihydroxy-1,1'-binaphthyl-boric acid In tetrahydrofuran; dichloromethane at -78℃; for 4h; | 99% |
With (R)-3,3'-di(2-hydroxyphenyl)-2,2'-dihydroxy-1,1'-binaphthyl*B(OMe)3 In tetrahydrofuran; dichloromethane at -78℃; for 4h; | 99% |
With 2,6-di-tert-butyl-pyridine; boron tribromide; (2S,5S)-N-2-hydroxybenzyl-2,5-dibenzylpyrrolidine In dichloromethane at -94℃; for 1h; Diels-Alder reaction; | 96% |
2-methylpropenal
ethyl acetate
Ethyl (+/-)-3-hydroxy-4-methyl-4-pentenoate
Conditions | Yield |
---|---|
Stage #1: ethyl acetate With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 0.333333h; Stage #2: 2-methylpropenal In tetrahydrofuran at -78℃; for 1h; | 99% |
With lithium diisopropyl amide In tetrahydrofuran | 91% |
With lithium diisopropyl amide In tetrahydrofuran; hexane at -60 - -30℃; for 0.833333h; | 91% |
2-methylpropenal
(E)-3-(tert-butyldimethylsiloxy)-1-(2-oxazolidinon-3-yl)-1,3-butadiene
Conditions | Yield |
---|---|
In toluene at 55℃; for 20h; Diels-Alder reaction; | 99% |
In chloroform-d1 at 22℃; Kinetics; Further Variations:; Solvents; temperature; Diels-Alder reaction; |
2-methylpropenal
cyclopenta-1,3-diene
(1S,2S,4S)-2-Methylbicyclo<2.2.1>hept-5-en-2-carbaldehyd
Conditions | Yield |
---|---|
With C66H29B2F30N2O6P In dichloromethane at -78℃; for 1h; Reagent/catalyst; Diels-Alder Cycloaddition; Schlenk technique; Inert atmosphere; Molecular sieve; enantioselective reaction; | 99% |
silver hexafluoroantimonate; [η6-cymene)RuCl(L4)]SbF6 In dichloromethane at -24℃; for 16h; | 95% |
Conditions | Yield |
---|---|
(S)-oxazaborolidine-aluminum bromide at -78℃; for 16h; Diels-Alder reaction; | 99% |
With trifluorormethanesulfonic acid; chiral oxazaborolidine In dichloromethane at -78℃; for 13h; Diels-Alder reaction; | 96% |
With aluminum tri-bromide; C24H22BF2NO In methanol at -10℃; Reagent/catalyst; Temperature; Diels-Alder Cycloaddition; enantioselective reaction; | n/a |
2-methylpropenal
Conditions | Yield |
---|---|
In dichloromethane stirring (5 min); removal of volatiles (vac.); | 99% |
2-methylpropenal
Conditions | Yield |
---|---|
In neat (no solvent) under dry N2 or Ar, using Schlenk techniques; excess neat methacrolein; pptd. with petroleum ether; | 99% |
2-methylpropenal
Conditions | Yield |
---|---|
In neat (no solvent) under dry N2 or Ar, using Schlenk techniques; excess neat methacrolein; pptd. with petroleum ether; | 99% |
2-methylpropenal
Conditions | Yield |
---|---|
With molecular sieves In dichloromethane byproducts: water; (Ar); addn. of an excess of methacrolein and molecular sieves to soln. of (S(Ir)R(C))-(η5-C5Me5)Ir(cyphos)(H2O)(SbF6)2 in CH2Cl2 at -25°C, stirring for 20 min; filtration through a cannula, concn., addn. of n-hexane, filtration, washing with n-hexane, vac.-drying; elem. anal.; | 99% |
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)dichloro[1,3-bis(1′-butylbenzimidazol-2′-yliden-3′-yl)benzene]dirhodium(I) In benzene-d6 at 20℃; for 20h; Catalytic behavior; Time; Reagent/catalyst; | 99% |
Conditions | Yield |
---|---|
With hydrogen In acetone at 20℃; under 760.051 Torr; for 0.25h; chemoselective reaction; | 99% |
With hydrogen; sodium triethylborohydride In tetrahydrofuran at 23℃; under 30402 Torr; for 72h; Catalytic behavior; Inert atmosphere; Schlenk technique; | 76% |
With hydrogen In ethyl acetate at 20℃; under 760.051 Torr; for 0.25h; chemoselective reaction; |
2-methylpropenal
2,3-dibromo-2-methylpropanal
Conditions | Yield |
---|---|
With bromine In dichloromethane at 20℃; for 2.5h; | 98% |
With bromine at 50℃; for 2h; | 60% |
With carbon disulfide; bromine | |
With bromine | |
With bromine In dichloromethane at 10℃; |
2-methylpropenal
2-methyl-2,3-dichloropropionaldehyde
Conditions | Yield |
---|---|
With chlorine at -5 - 0℃; for 1.5h; Neat (no solvent); | 98% |
With chlorine at 50℃; for 2h; | 76% |
With chlorine | |
With chlorine |
2-methylpropenal
cyclopenta-1,3-diene
exo-2-methylbicyclo[2.2.1]hept-5-ene-2-carbaldehyde
Conditions | Yield |
---|---|
With C31H28BNO; tin(IV) chloride In dichloromethane at -78℃; for 2h; Reagent/catalyst; Diels-Alder Cycloaddition; Reflux; stereoselective reaction; | 98% |
With 2,2'-bis(dibenzo[a,c]-1,3,2-dioxaborepin-2-yloxy)biphenyl In dichloromethane at -78℃; for 24h; Diels-Alder reaction; | 97% |
With bis<2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)phenolato-N,O>-zirconium(IV) triflate In dichloromethane at -78 - 20℃; | 75% |
Reported in EPA TSCA Inventory.
DOT Classification: 3; Label: Flammable Liquid, Poison
The Methylacrylaldehyde with CAS registry number of 78-85-3 is also known as 2-Methyl-2-propen-1-al. The IUPAC name is 2-Methylprop-2-enal. Its EINECS registry number is 201-150-1. In addition, the formula is C4H6O and the molecular weight is 70.09. This chemical is a colourless to light yellow liquid and should be sealed in dry and cool place.
Physical properties about Methylacrylaldehyde are: (1)ACD/LogP: 0.54; (2)ACD/LogD (pH 5.5): 0.54; (3)ACD/LogD (pH 7.4): 0.54; (4)ACD/BCF (pH 5.5): 1.52; (5)ACD/BCF (pH 7.4): 1.52; (6)ACD/KOC (pH 5.5): 46.99; (7)ACD/KOC (pH 7.4): 46.99; (8)#H bond acceptors: 1; (9)#Freely Rotating Bonds: 1; (10)Index of Refraction: 1.384; (11)Molar Refractivity: 20.33 cm3; (12)Molar Volume: 86.7 cm3; (13)Surface Tension: 20.8 dyne/cm; (14)Density: 0.807 g/cm3; (15)Enthalpy of Vaporization: 30.98 kJ/mol; (16)Boiling Point: 68 °C at 760 mmHg; (17)Vapour Pressure: 142 mmHg at 25 °C.
Preparation of Methylacrylaldehyde: it is prepared by reaction of at least one of isobutylene and tert-butyl alcohol. The gas containing molecular oxygen is oxidated in presence of oxidation catalyst Mo12BiaCebKcFedAeBfOg.
Uses of Methylacrylaldehyde: it is used for the manufacture of copolymers and resins, and also is the raw material of methylmalonic acid and thermoplastic fuel. It is used to produce 2,3-dibromo-2-methyl-propionaldehyde. The reaction occurs with reagent bromine at 50 °C for 2 hours. The yield is about 60%.
When you are using this chemical, please be cautious about it. As a chemical, it is toxic in contact with skin and if swallowed and very toxic by inhalation. What's more, it is highly flammable that can cause burns. During using it, wear suitable protective clothing, gloves and eye/face protection. Keep away from sources of ignition. If accident happens or you feel unwell seek medical advice immediately. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
You can still convert the following datas into molecular structure:
1. Canonical SMILES: CC(=C)C=O
2. InChI: InChI=1S/C4H6O/c1-4(2)3-5/h3H,1H2,2H3
3. InChIKey: STNJBCKSHOAVAJ-UHFFFAOYSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rabbit | LD50 | skin | 430uL/kg (0.43mL/kg) | Journal of Industrial Hygiene and Toxicology. Vol. 31, Pg. 60, 1949. | |
rat | LCLo | inhalation | 125ppm/4H (125ppm) | Journal of Industrial Hygiene and Toxicology. Vol. 31, Pg. 343, 1949. | |
rat | LD50 | oral | 140mg/kg (140mg/kg) | Union Carbide Data Sheet. Vol. 7/21/1965, |
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