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NAME:P-ANISALDEHYDE DIMETHYL ACETAL
CAS NO£º2186-92-7
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²Ñ°Â£º182.22
·¡±õ±··¡°ä³§£º218-577-4
BP: 85-87 ¡ãC0.1 mm Hg(lit.)
DENSITY: 1.07 g/mL at 20 ¡ãC(lit.)
FP: 97¡ãC
Name: P-ANISALDEHYDE DIMETHYL ACETAL
CAS NO£º2186-92-7
MF£ºC10H14O3
MW£º182.22
EINECS£º218-577-4
BP: 85-87 ¡ãC0.1 mm Hg(lit.)
DENSITY: 1.07 g/mL at 20 ¡ãC(lit.)
FP: 97¡ãC
³§°Õ°¿¸é´¡³Ò·¡:2-8¡ã°ä&²Ô²ú²õ±è;&²Ô²ú²õ±è;
Purity: 97% min
Appearance: Clear colorless to light yellow Liquid
Package: 25g, 100g, 500g, bulk package
Application:Organic intermediates
Other name:
1-(Dimethoxymethyl)-4-methoxybenzol;
4-METHOXYBENZALDEHYDE DIMETHYL ACETAL;
Anisaldehyde dimethyl acetal;
Benzene, 1-(dimethoxymethyl)-4-methoxy-;
4-Methoxybenzaldehyde dimethyl acetal CAS NO£º2186-92-7 is used as a precursor to 1-methoxy-1-(4-methoxyphenyl)hept-2-yne, 2,5-dioxopyrrolidin-1-yl-3-((4R)-2-(4-methoxyphenyl)-5,5-dimethyl-1,3-dioxane-4-carboxamido)propanoate and 1-(p-anisyl)-2-(2-methoxyethyl)-3-phenylindene. Further, it acts as a protecting group reagent for diols, especially in carbohydrates. It is also used as a flavor essence in sunflower, cyclamen and in jasmine. In addition to this, it is involved in allylation reactions with allyltrimethylsilane catalyzed by Iron(III) chloride.
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