All Photos(1)
About This Item
Linear Formula:
C6H5CO2CH2C≡CH
CAS Number:
Molecular Weight:
160.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
liquid
refractive index
n20/D 1.5320 (lit.)
bp
225-226 °C (lit.)
density
1.106 g/mL at 25 °C (lit.)
SMILES string
O=C(OCC#C)c1ccccc1
InChI
1S/C10H8O2/c1-2-8-12-10(11)9-6-4-3-5-7-9/h1,3-7H,8H2
InChI key
NBDHEMWCIUHARG-UHFFFAOYSA-N
Related Categories
General description
Propargyl benzoate is an aromatic ester containing a terminal acetylene group. It can be synthesized by reacting propargyl bromide and benzoyl chloride.
Application
Propargyl benzoate may be used in the preparation of amphiphilic graft copolymers of poly(ε-caprolactone) (PCL).
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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.
Nickel-Catalyzed Tandem Coupling of ?,?-Enones, Alkynes, and Alkynyltins for the Regio-and Stereoselective Synthesis of Conjugated Enynes.
Ikeda S, et al.
The Journal of Organic Chemistry, 61(23), 8248-8255 (1996)
Combination of ring-opening polymerization and ?click chemistry?: toward functionalization and grafting of poly (?-caprolactone).
Riva R, et al.
Macromolecules, 40(4), 796-803 (2007)
Articles
New Aromatic Terminal Alkynes
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