Allyl benzyl ether

Inquiry

Molecular Formula:

C10H12O

Molecular Weight:

148.20

CAS Number:

14593-43-2

Catalog Number:

14593-43-2

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

204-205ºC

Flash Point

76 ℃

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

Hydrogen Bond Acceptor Count

Rotatable Bond Count

Exact Mass

148.088815002 g/mol

Monoisotopic Mass

148.088815002 g/mol

Topological Polar Surface Area

9.2Å²

Heavy Atom Count

Formal Charge

Complexity

103

Isotope Atom Count

Defined Atom Stereocenter Count

Undefined Atom Stereocenter Count

Defined Bond Stereocenter Count

Undefined Bond Stereocenter Count

Covalently-Bonded Unit Count

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)

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The dilution calculator equation

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

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

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Volume _(start)

Concentration _(final)

Volume _(final)