Allyl benzyl ether

Product Information

Molecular Formula:
C10H12O
Molecular Weight:
148.20
Description
Applications: ((allyloxy)methyl)benzene is a useful research chemical.
Synonyms
ALLYL BENZYL ETHER; alpha-(allyloxy)toluene; (Allyloxymethyl)benzene; [(Allyloxy)methyl]benzene; 2-Propenyl benzyl ether; Benzyl 2-propenyl ether
IUPAC Name
prop-2-enoxymethylbenzene
Canonical SMILES
C=CCOCC1=CC=CC=C1
InChI
InChI=1S/C10H12O/c1-2-8-11-9-10-6-4-3-5-7-10/h2-7H,1,8-9H2
InChI Key
HUGHWHMUUQNACD-UHFFFAOYSA-N
Boiling Point
204-205°C
Flash Point
76 °C
Purity
95%
Density
0.959
Appearance
Colorless to Almost colorless clear liquid
Refractive Index
n20/D 1.507 (lit.)

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].

Computed Properties

XLogP3
2.6
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
4
Exact Mass
148.088815002 g/mol
Monoisotopic Mass
148.088815002 g/mol
Topological Polar Surface Area
9.2Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
103
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114133410-A Oligomeric siloxane containing accelerant and cationic polymerizable group, preparation and application thereof 2021-12-07
DE-102020124036-A1 Stabilizer system containing sulfide for thiol-ene and thiol-yne compositions 2020-09-15
WO-2022042841-A1 Curable compositions and articles prepared therefrom 2020-08-27
CN-111939926-A Cu-Zr oxide nanoparticle loaded Pd (II) catalyst and preparation method and application thereof 2020-07-31
WO-2022024067-A1 Process for production of ascarylose and related compounds 2020-07-31
JP-2021197499-A Thermoelectric conversion materials and thermoelectric conversion elements 2020-06-17
CN-113755046-A Composition for encapsulating organic light emitting diode and organic light emitting diode display including organic layer formed therefrom 2020-06-03
JP-2021190428-A An organic light emitting display device containing a composition for encapsulating an organic light emitting element and an organic layer produced by the composition. 2020-06-03
KR-20210150021-A Composition for encapsulating organic light emitting diodes and organic light emitting diodes display comprising organic layer prepared using the same 2020-06-03
JP-2021190700-A Polyimide resin etching method 2020-05-29

Literatures

PMID Publication Date Title Journal
20845958 2010-10-13 Enantioselective hydroformylation of N-vinyl carboxamides, allyl carbamates, and allyl ethers using chiral diazaphospholane ligands Journal of the American Chemical Society
18686280 2008-01-01 Highly regioselective hydroformylation with hemispherical chelators Chemistry (Weinheim an der Bergstrasse, Germany)
18078507 2007-12-13 Part 3. Triethylborane-air: a suitable initiator for intermolecular radical additions of S-2-oxoalkyl-thionocarbonates (S-xanthates) to olefins Beilstein journal of organic chemistry
12120389 2002-02-07 A new and short method for the synthesis of 2,4-methanoproline Chemical communications (Cambridge, England)
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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