163953
3-Benzyloxy-4-methoxybenzaldehyde
98%
Sign Into View Organizational & Contract Pricing
About This Item
Linear Formula:
C6H5CH2OC6H3(OCH3)CHO
CAS Number:
Molecular Weight:
242.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Quality Level
Assay
98%
form
solid
mp
61-64 °C (lit.)
functional group
aldehyde
phenyl
SMILES string
COc1ccc(C=O)cc1OCc2ccccc2
InChI
1S/C15H14O3/c1-17-14-8-7-13(10-16)9-15(14)18-11-12-5-3-2-4-6-12/h2-10H,11H2,1H3
InChI key
VQVQZFHUXRSRBZ-UHFFFAOYSA-N
Application
3-Benzyloxy-4-methoxybenzaldehyde was used in the synthesis of (+)-9-benzyloxy-α-dihydrotetrabenazine. It was also used in total synthesis of (-)-galipeine.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Chunyi Liu et al.
Chirality, 25(4), 215-223 (2013-03-28)
This article reports, for the first time, on the absolute configuration of (+)-9-benzyloxy-α-dihydrotetrabenazine (8), as determined from the perspective of X-ray crystallography. Compound 8 was prepared by a six-step reaction using 3-benzyloxy-4-methoxybenzaldehyde (1) as a starting material. The X-ray crystal
The enantioselective total synthesis of alkaloid (-)-galipeine.
Yang P-Y and Zhou Y-G.
Tetrahedron Asymmetry, 15(7), 1145-1149 (2004)
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