All Photos(1)
Linear Formula:
H2C=C(CH3)CH2CH2CO2C2H5
CAS Number:
Molecular Weight:
142.20
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
95%
form
liquid
refractive index
n20/D 1.425 (lit.)
bp
85 °C/20 mmHg (lit.)
density
0.891 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)CCC(C)=C
InChI
1S/C8H14O2/c1-4-10-8(9)6-5-7(2)3/h2,4-6H2,1,3H3
InChI key
RRTBSPBUHUUTHR-UHFFFAOYSA-N
Related Categories
General description
Ethyl 4-methyl-4-pentenoate is an olefin ester. It undergoes iron carbonyl-promoted isomerization to α,β-unsaturated esters. Reaction of ethyl 4-methyl-4-pentenoate with CH3OBOCH3+ was examined in a small Fourier-transform ion cyclotron resonance mass spectrometer equipped with a permanent magnet.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Flam. Liq. 3
WGK
WGK 3
Flash Point(F)
136.4 °F
Flash Point(C)
58 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
K K Thoen et al.
Journal of the American Society for Mass Spectrometry, 7(11), 1138-1143 (1996-11-01)
The usefulness of CH3OBOCH 3 (+) as a chemical ionization reagent was examined by allowing the ion to react with carboxylic esters of various chain lengths in a small Fourier-transform ion cyclotron resonance mass spectrometer equipped with a permanent magnet.
Kuo-Chen Shih et al.
The Journal of organic chemistry, 61(22), 7784-7792 (1996-11-01)
Ultraviolet photolysis of stoichiometric amounts of methyl oleate and Fe(CO)(5) in hexanes solvent at 0 degrees C gives Fe(CO)(3)(eta(4)-alpha,beta-ester) in which the alpha,beta-unsaturated ester isomer of methyl oleate is stabilized by eta(4)-oxadiene pi coordination of the olefin and ester carbonyl
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service