137243
4-(p-Tolyl)-3-buten-2-one
(predominantly trans), 97%
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About This Item
Linear Formula:
CH3C6H4CH=CHCOCH3
CAS Number:
Molecular Weight:
160.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
form
solid
composition
(predominantly trans)
mp
29-33 °C (lit.)
SMILES string
CC(=O)\C=C\c1ccc(C)cc1
InChI
1S/C11H12O/c1-9-3-6-11(7-4-9)8-5-10(2)12/h3-8H,1-2H3/b8-5+
InChI key
USXMUOFSQBSHGN-VMPITWQZSA-N
General description
4-(p-Tolyl)-3-buten-2-one undergoes Reformatsky reaction with ethyl α-bromopropionate to yield β-hydroxy esters.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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Geometric Isomers of 2, 3-Dimethyl-5-aryl-2, 4-pentadienoic Acids. The Steric Factors Favoring 2-cis Formation.
Wiley RH, et al.
The Journal of Organic Chemistry, 29(10), 2986-2990 (1964)
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