ChemicalBook Product Catalog Chemical Reagents Organic reagents Aliphatic aldehydes P-ANISALDEHYDE DIMETHYL ACETAL

P-ANISALDEHYDE DIMETHYL ACETAL

P-ANISALDEHYDE DIMETHYL ACETAL Basic information
Product Name:P-ANISALDEHYDE DIMETHYL ACETAL
Synonyms:1-(dimethoxymethyl)-4-methoxy-benzen;1-(dimethoxymethyl)-4-methoxy-Benzene;P-ANISALDEHYDE DIMETHYL ACETAL;Anisicaldehydedimethylacetal;4-METHOXYBENZALDEHYDE DIMETHYL ACETAL;ANISALDEHYDE DIMETHYL ACETAL;ANISIC ALDEHYDE DMA;p-(dimethoxymethyl)anisole
CAS:2186-92-7
MF:C10H14O3
MW:182.22
EINECS:218-577-4
Product Categories:Biochemistry;Reagents for Oligosaccharide Synthesis
Mol File:2186-92-7.mol
P-ANISALDEHYDE DIMETHYL ACETAL Structure
P-ANISALDEHYDE DIMETHYL ACETAL Chemical Properties
Boiling point 85-87 °C0.1 mm Hg(lit.)
density 1.07 g/mL at 20 °C(lit.)
vapor pressure 2.407-48Pa at 25-61.2℃
refractive index n20/D 1.505
Fp 97°C
storage temp. 2-8°C
solubility H2O: soluble
form Liquid
color Clear colorless to light yellow
Odorat 100.00 %. mild floral hawthorn jasmin lilac elderflower
Odor Typefloral
Water Solubility Miscible with alcohol and many organic solvents. Slightly miscible with water.
BRN 2048930
LogP2 at 25℃
CAS DataBase Reference2186-92-7(CAS DataBase Reference)
EPA Substance Registry Systemp-(Dimethoxymethyl)anisole (2186-92-7)
Safety Information
Safety Statements 24/25
WGK Germany 1
F 10
TSCA Yes
HS Code 29110000
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
P-ANISALDEHYDE DIMETHYL ACETAL Usage And Synthesis
Chemical Propertiesclear colorless to light yellow liquid
Uses4-Methoxybenzaldehyde dimethyl acetal 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.
1,3-DiMethyl 2-[4-(Methoxycarbonyl)-2-nitrophenyl]propanedioate 3,4,6-TRIMETHOXY-1(3H)-ISOBENZOFURANONE P-ANISALDEHYDE DIETHYL ACETAL RARECHEM AL BP 0548 RARECHEM AL BP 0187 RARECHEM AL BP 0176 3,4,5-TRIMETHOXYBENZALDEHYDE DIMETHYL ACETAL BIS-(3,4,5-TRIMETHOXYPHENYL)-1,3-DIOXOLANE 1-BROMO-5-(1,3-DIOXOLAN-2-YL)-2-METHOXYBENZENE 5-DIMETHOXYMETHYL-BENZO[1,3]DIOXOLE HELIOTROPINE DIETHYL ACETAL 3,3-BIS(HYDROXYMETHYL)-2,3-DIHYDRO-4H-THIOCHROMEN-4-ONE 4-METHOXYBENZALDEHYDE ACETAL 2,6-Bis(4-methoxyphenyl)-2-methyl-4H-1,3-dioxin-4-one TIMTEC-BB SBB012300 P-ANISALDEHYDE DIMETHYL ACETAL, (4-METHOXYBENZALDEHYDE DIMETHYL ACETAL) 3,4-diacetoxybenzylidene diacetate PIPROTAL (+/-) CIS-2,5-BIS(3,4,5-TRIMETHOXYPHENYL)-1,3-DIOXOLANE Anisaldehyde Dimethyl Acetal
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