499749
2-Benzyloxybenzaldehyde
98%
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About This Item
Linear Formula:
C6H5CH2OC6H4CHO
CAS Number:
Molecular Weight:
212.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
2-Benzyloxybenzaldehyde, 98%
InChI
1S/C14H12O2/c15-10-13-8-4-5-9-14(13)16-11-12-6-2-1-3-7-12/h1-10H,11H2
SMILES string
O=Cc1ccccc1OCc2ccccc2
InChI key
PBEJTRAJWCNHRS-UHFFFAOYSA-N
assay
98%
refractive index
n20/D 1.6 (lit.)
bp
326 °C (lit.)
density
1.339 g/mL at 25 °C (lit.)
Application
2-Benzyloxybenzaldehyde may be used in the synthesis of:
- 2-benzyloxy-2′-hydroxy-3′,4′,6′-trimethoxychalcone
- N2-(2-benzyloxy)benzylidenyl isonicotinic acid hydrazide
- 2-hydroxy-2′-methoxybenzophenone
- 2′-hydroxy-5,6,7-trimethoxyflavone
General description
2-Benzyloxybenzaldehyde is a benzaldehyde derivative. It undergoes enantioselective cyanoformylation with ethyl cyanoformate in the presence of a vanadium(V) chiral salen complex and imidazole to form the corresponding cyanohydrin carbonate.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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Synthesis of 3-ureido derivatives of coumarin and 2-quinolone as potent acyl-CoA: cholesterol acyltransferase inhibitors.
Tawada H, et al.
Chemical & Pharmaceutical Bulletin, 43(4), 616-625 (1995)
The synthesis of 5, 2'-dihydroxy-6, 8-dimethoxyflavone and its isomers: A revised structure of skullcapflavone I.
Horie T, et al.
Bulletin of the Chemical Society of Japan, 52(10), 2950-2952 (1979)
Vanadium(V) salen complex catalyzed highly enantioselective cyanoformylation of aldehydes in the presence of imidazole as a cocatalyst.
Khan NH, et al.
European Journal of Organic Chemistry, 2008(26), 4511-4515 (2008)
Synthesis and structure-activity relationship of cytotoxic 5,2',5'-trihydroxy-7,8-dimethoxyflavanone analogues.
Min BS, et al.
Archives of Pharmacal Research, 19(6), 543-550 (1996)
Michael J Hearn et al.
European journal of medicinal chemistry, 44(10), 4169-4178 (2009-06-16)
Structural modification of the frontline antitubercular isonicotinic acid hydrazide (INH) provides lipophilic adaptations (3-46) of the drug in which the hydrazine moiety of the parent compound has been chemically blocked from the deactivating process of N(2)-acetylation by N-arylaminoacetyl transferases. As
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