195863
2,3,4-Trimethoxybenzyl alcohol
97%
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About This Item
Linear Formula:
(CH3O)3C6H2CH2OH
CAS Number:
Molecular Weight:
198.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
276-270-0
MDL number:
Product Name
2,3,4-Trimethoxybenzyl alcohol, 97%
InChI key
DGJVVEVPKPOLEV-UHFFFAOYSA-N
InChI
1S/C10H14O4/c1-12-8-5-4-7(6-11)9(13-2)10(8)14-3/h4-5,11H,6H2,1-3H3
SMILES string
COc1ccc(CO)c(OC)c1OC
assay
97%
form
liquid
refractive index
n20/D 1.532 (lit.)
bp
105 °C/25 mmHg (lit.)
density
1.151 g/mL at 25 °C (lit.)
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Application
2,3,4-Trimethoxybenzyl alcohol was used to introduce a benzyl group onto the 2′-OH of purine ribonucleoside.
General description
Photoelectrocatalytic partial oxidation of 2,3,4-trimethoxybenzyl alcohol in aqueous solution irradiated by near-UV light has been investigated in three-electrode batch reactor.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Photoelectrocatalytic selective oxidation of 4-methoxybenzyl alcohol in water by TiO2 supported on titanium anodes.
Ozcan L, et al.
Applied Catalysis. B, Environmental, 132, 535-542 (2013)
Shigetada Kozai et al.
Nucleosides, nucleotides & nucleic acids, 22(2), 145-151 (2003-05-15)
A new method to introduce a benzyl group onto the 2'-OH of purine ribonucleoside is described. Thus, 6-chloropurine 3'-O-benzoylriboside and its 5'-O-trityl congener were condensed with benzyl alcohol using the Mitsunobu reaction to give the 2'-O-benzyl derivative. The yields were
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