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About This Item
Linear Formula:
C6H5COCH=CHCO2C2H5
CAS Number:
Molecular Weight:
204.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
grade
technical grade
Quality Level
Assay
92%
form
liquid
refractive index
n20/D 1.543 (lit.)
bp
184-185 °C/25 mmHg (lit.)
density
1.112 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)\C=C\C(=O)c1ccccc1
InChI
1S/C12H12O3/c1-2-15-12(14)9-8-11(13)10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+
InChI key
ACXLBHHUHSJENU-CMDGGOBGSA-N
Related Categories
General description
Ethyl 3-benzoylacrylate (ethyl trans-3-benzoylacrylate) undergoes enantioselective guanidine catalyst promoted Michael addition reaction with dithranol to yield Michael adduct.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
235.4 °F
Flash Point(C)
113 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Juan Shen et al.
Organic & biomolecular chemistry, 6(18), 3229-3236 (2008-09-20)
The enantioselective Diels-Alder reaction is one of the most important reactions for the synthesis of complex molecules. It provides access to chiral six-membered carbocyclic compounds containing up to four stereogenic centers in a single step. Asymmetric catalysis in the Diels-Alder
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