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543985

Sigma-Aldrich

Propargyl benzoate

98%

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5 G
HUF 12,300.00

HUF 12,300.00

List PriceHUF 24,600.00Save 50%
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5 G
HUF 12,300.00

About This Item

Linear Formula:
C6H5CO2CH2C≡CH
CAS Number:
6750-04-5
Molecular Weight:
160.17
MDL number:
MFCD00996341
UNSPSC Code:
12352100
PubChem Substance ID:
24878282
NACRES:
NA.22

HUF 12,300.00

List PriceHUF 24,600.00Save 50%
Please contact Customer Service for Availability
Request a Bulk Order

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.)

functional group

ester
phenyl

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

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This Item
348155B6630543136
Propargyl benzoate 98%

543985

Propargyl benzoate

Methyl 4-(bromomethyl)benzoate 98%

348155

Methyl 4-(bromomethyl)benzoate

Benzyl benzoate ReagentPlus®, ≥99.0%

B6630

Benzyl benzoate

Propargyl acrylate 98%

543136

Propargyl acrylate

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

bp

225-226 °C (lit.)

bp

130-135 °C/2 mmHg (lit.)

bp

323-324 °C (lit.)

bp

142-143 °C (lit.)

density

1.106 g/mL at 25 °C (lit.)

density

-

density

1.118 g/mL at 20 °C (lit.)

density

0.997 g/mL at 25 °C (lit.)

refractive index

n20/D 1.5320 (lit.)

refractive index

-

refractive index

n20/D 1.568 (lit.)

refractive index

n20/D 1.447 (lit.)

form

liquid

form

-

form

liquid

form

-

General description

Propargyl benzoate is an aromatic ester containing a terminal acetylene group. It can be synthesized by reacting propargyl bromide and benzoyl chloride.[1]

Application

Propargyl benzoate may be used in the preparation of amphiphilic graft copolymers of poly(ε-caprolactone) (PCL).[2]

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS3592
MKCN7863
MKCN6142
MKBK4179V
MKBJ9926V

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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)
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)

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