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pd_proNo:464389-dbe62610-d4f4-43a0-a185-2aee1d2b522c
pd_productuse:
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Preparation |
By direct esterification of anisic alcohol with formic acid. |
|
Flammability and Explosibility |
Notclassified |
|
Metabolism |
Esters of benzyl alcohol, such as the acetate, are rapidly hydrolysed in vivo to benzyl alcohol, which is then oxidized. The expected general reaction of primary aromatic alcohols in the animal body is oxidation to the corresponding aromatic acid, which is usually excreted as a glycine conjugate and to a lesser extent as an ester glucuronide. In rabbits, benzyl alcohol is almost entirely converted to benzoic acid, which is excreted mainly as hippuric acid . In substituted anisoles with a carboxyl group or a potential carboxyl group attached to the aromatic ring, the ether link is relatively stable(Williams, 1959). |
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Aroma threshold values |
Odor characteristics are sweet, spicy, vanilla-like with powdery fruity nuances. |
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Taste threshold values |
Taste characteristics at 50 ppm: sweet, vanilla, spice, with fruity heliotropine-like nuances. |
InChI:InChI=1/C9H10O3/c1-11-9-4-2-8(3-5-9)6-12-7-10/h2-5,7H,6H2,1H3
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The invention discloses a method for pre...
Herein, formylation of structurally diff...
In this work, nanoporous sodium montmori...
1,4-di(4-methoxyphenyl)ethanone
ethanol
p-methylanizole
ethyl 4-methoxybenzoate
4-methoxy-, benzenemethanol, formate
4-methoxy-benzaldehyde
p-ethylanisole
Diethyl maleate
succinic acid diethyl ester
| Conditions | Yield |
|---|---|
|
With
[methyl-3-(butyl-4-sulfonate) imidazolium]CuPW12O40; oxygen;
at 159.84 ℃;
for 5h;
under 6000.6 Torr;
|
4-Methoxybenzyl alcohol
formic acid ethyl ester
4-methoxy-, benzenemethanol, formate
| Conditions | Yield |
|---|---|
|
With
K5
|
98% |
|
With
Silphos;
at 20 ℃;
for 0.0833333h;
|
98% |
|
(NH4)8[CeW10O36]*20H2O;
for 3h;
Heating;
|
95% |
|
With
silica-bonded N-propyl sulfamic acid;
at 20 ℃;
for 0.5h;
chemoselective reaction;
|
94% |
|
With
sulfonic acid supported on polydopamine (PDA)-encapsulated Fe3O4 nanoparticles;
In
neat (no solvent);
at 40 ℃;
for 1h;
Green chemistry;
|
90% |
formamide
4-Methoxybenzyl alcohol
formic acid
4-formyloxy-1-[1'-(4-methoxybenzyloxy)propan-3'-yl]azetidin-2-one
6-phenyl-3a,4-dihydro-1H-cyclopenta[c]furan-5(3H)-one
methanol
4,4'-dimethoxydibenzyl ether
4-Methoxybenzyl alcohol
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