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About This Item
Linear Formula:
H2C=CHCH2OC6H4CHO
CAS Number:
Molecular Weight:
162.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
refractive index
n20/D 1.568 (lit.)
bp
150-152 °C/18 mmHg (lit.)
density
1.058 g/mL at 25 °C (lit.)
SMILES string
C=CCOc1ccc(C=O)cc1
InChI
1S/C10H10O2/c1-2-7-12-10-5-3-9(8-11)4-6-10/h2-6,8H,1,7H2
InChI key
TYNJQOJWNMZQFZ-UHFFFAOYSA-N
General description
4-Allyloxybenzaldehyde can be prepared by reacting 4-hydroxybenzaldehyde and allylbromide in the presence of a base.4 It can undergo chemoselective dithioacetalization in the presence of cobalt(II)chloride.
Application
4-Allyloxybenzaldehyde may be used in the preparation of:
- 4,6,4′,6′-O-di-4-allyloxybenzylidene-α,α-D-trehalose
- 3-allyl-4-hydroxybenzaldehyde
- (±)-4-allyloxymethamphetamine (ALLMA)
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Sens. 1
Storage Class Code
12 - Non 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’.
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Selective mechanism-based inactivation of rat CYP2D by 4-allyloxymethamphetamine.
Lin LY, et al.
Journal of Pharmacology and Experimental Therapeutics, 277(2), 595-603 (1996)
Synthesis and properties of thermoplastic alternating copolymers containing trehalose and siloxane units by hydrosilylation reaction.
Teramoto N, et al.
Polymer Journal, 39(9), 975-975 (2007)
An isomerization-ring-closing metathesis strategy for the synthesis of substituted benzofurans.
van Otterlo WAL, et al.
Tetrahedron, 61(32), 7746-7755 (2005)
Cobalt (II) chloride catalyzed chemoselective thioacetalization of aldehydes.
De SK.
Tetrahedron Letters, 45(5), 1035-1036 (2004)
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