• Name

  2-ethyl-3-methylbutyraldehyde

• EINECS 247-551-5
• CAS No. 26254-92-2
• Article Data11
• CAS DataBase
• Density 0.803 g/cm³
• Solubility
• Melting Point 128-132 °C
• Formula C₇H₁₄O
• Boiling Point 134 °C
• Molecular Weight 114.188
• Flash Point 33 °C
• Transport Information
• Appearance
• Safety
• Risk Codes
• Molecular Structure
• Hazard Symbols
• Synonyms Butyraldehyde,2-ethyl-3-methyl- (6CI,7CI,8CI);(?à)-2-Isopropylbutyraldehyde;2-Ethyl-3-methylbutanal;2-Ethyl-3-methylbutyraldehyde;2-Isopropylbutanal;
• PSA 17.07000
• LogP 1.86750

Synthetic route

855742-28-8

methoxymethyl-ethyl-isopropyl-carbinol

26254-92-2

α-ethylisovaleraldehyde

Conditions

Conditions	Yield
With oxalic acid at 100 - 105℃;

51760-89-5

2-ethyl-3-methyl-butyryl chloride

26254-92-2

α-ethylisovaleraldehyde

Conditions

Conditions	Yield
Hydrogenation;

855742-28-8

methoxymethyl-ethyl-isopropyl-carbinol

144-62-7

oxalic acid

26254-92-2

α-ethylisovaleraldehyde

Conditions

Conditions	Yield
at 100 - 105℃;

75-03-6

ethyl iodide

590-86-3

isovaleraldehyde

26254-92-2

α-ethylisovaleraldehyde

Conditions

Conditions	Yield
(i) nBu3SnOMe, Et2O, (ii) /BRN= 505934/; Multistep reaction;

64-17-5

ethanol

20817-72-5, 55722-32-2, 83603-21-8

(22E)-stigmasta-4,22-dien-3-one

A

26254-92-2

α-ethylisovaleraldehyde

B

3986-89-8

(20S)-3-oxopregn-4-ene-20-carboxaldehyde

C

76692-30-3

3-Oxobisnor-4-cholenaldehyde diethyl acetal

Conditions

Conditions	Yield
With dimethylsulfide; ozone Solvent Red 23 (Table 2), CH2Cl2; Yield given. Multistep reaction. Yields of byproduct given;

...Expand

(1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Ethoxy-6-((E)-(S)-4-ethyl-1,5-dimethyl-hex-2-enyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene

A

26254-92-2

α-ethylisovaleraldehyde

B

(20 S)-6β-ethoxy-3α,5-cyclo-5α-pregnane-20-carbaldehyde

Conditions

Conditions	Yield
With diphenylphosphinopolystyrene; oxygen; ozone; triphenylphosphine 1.) CH2Cl2, -78 deg C, 3 min, 2.) -> RT; RT, 30 min; Yield given. Multistep reaction;
With diphenylphosphinopolystyrene; oxygen; ozone; triphenylphosphine Product distribution; 1.) CH2Cl2, -78 deg C, 2.) RT;

ethylisopropylacetyl chloride

ethylisopropylacetyl chloride

26254-92-2

α-ethylisovaleraldehyde

Conditions

Conditions	Yield
Hydrogenation.katalytische Hydrierung;

65857-35-4

1-methoxy-3-methyl-butan-2-one

26254-92-2

α-ethylisovaleraldehyde

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: diethyl ether 2: oxalic acid / 100 - 105 °C View Scheme

592-41-6

1-hexene

201230-82-2

carbon monoxide

A

111-71-7

heptanal

B

1860-39-5

5-methylhexanal

C

925-54-2

2-methylhexanal

D

26254-92-2

α-ethylisovaleraldehyde

Conditions

Conditions	Yield
With hydrogen In Tridecane; toluene at 80℃; Kinetics; Temperature; Pressure; Autoclave;

...Expand

592-41-6

1-hexene

201230-82-2

carbon monoxide

A

111-71-7

heptanal

B

592-47-2

3-hexene

C

26254-92-2

α-ethylisovaleraldehyde

D

592-43-8

2-hexene

Conditions

Conditions	Yield
With hydrogen In toluene at 100℃; under 30003 Torr; Autoclave;

...Expand

26254-92-2

α-ethylisovaleraldehyde

56006-49-6, 32444-32-9

2-ethyl-3-methyl-butyric acid

Conditions

Conditions	Yield
With potassium permanganate
With potassium permanganate; sulfuric acid

26254-92-2

α-ethylisovaleraldehyde

67-64-1

acetone

50767-76-5, 51729-97-6

(R,S)-5-ethyl-6-methyl-(3E)-hepten-2-one

Conditions

Conditions	Yield
With potassium hydroxide Heating;

26254-92-2

α-ethylisovaleraldehyde

51760-89-5

2-ethyl-3-methyl-butyryl chloride

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: potassium permanganate 2: thionyl chloride View Scheme
Multi-step reaction with 2 steps 1: KMnO4, aq. H2SO4 2: SOCl2 View Scheme

26254-92-2

α-ethylisovaleraldehyde

41654-25-5

(+/-)-3-Hydroxy-3-methyl-6-isopropyl-4-octensaeure-methylester

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: aq. KOH / Heating 2: Zn / benzene / Heating View Scheme

26254-92-2

α-ethylisovaleraldehyde

686267-68-5

1-amino-3-(1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl)-4-hydroxy-2(1H)-quinolinone

3-(1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl)-1-{[2-ethyl-3-methylbutylidene]amino}-4-hydroxyquinolin-2(1H)-one

Conditions

Conditions	Yield
In N,N-dimethyl acetamide at 110℃; for 0.583333h; Microwave irradiation;

2-Isopropylbutanal Specification