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p-Anisaldehyde dimethyl acetal

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p-Anisaldehyde dimethyl acetal manufacturers

p-Anisaldehyde dimethyl acetal Basic information
Product Name:p-Anisaldehyde dimethyl acetal
Synonyms:1-(dimethoxymethyl)-4-methoxy-benzen;1-(dimethoxymethyl)-4-methoxy-Benzene;Anisicaldehydedimethylacetal;4-METHOXYBENZALDEHYDE DIMETHYL ACETAL;ANISIC ALDEHYDE DMA;p-(dimethoxymethyl)anisole;Benzene, 1-(dimethoxymethyl)-4-methoxy-;Anisaldehyddimethylacetal
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
OdorHerbal-green, somewhat floral odor, suggestive of Lilac (“Lilac-green’”), Hyacinth, Appleblossom, etc.
Odor Typefloral
Water Solubility Miscible with alcohol and many organic solvents. Slightly miscible with water.
BRN 2048930
InChI1S/C10H14O3/c1-11-9-6-4-8(5-7-9)10(12-2)13-3/h4-7,10H,1-3H3
InChIKeyNNHYAHOTXLASEA-UHFFFAOYSA-N
SMILESCOC(OC)c1ccc(OC)cc1
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
10
TSCA TSCA listed
HS Code 29110000
Storage Class10 - Combustible liquids
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.
SynthesisP-Anisaldehyde diMethyl acetal is produced from Anisaldehyde and Methyl alcohol.
Tag:p-Anisaldehyde dimethyl acetal(2186-92-7) Related Product Information
1-Chloro-4-(trimethoxymethyl)benzene 1,3-DiMethyl 2-[4-(Methoxycarbonyl)-2-nitrophenyl]propanedioate (Z)-methyl 3-(((4-(methylamino)phenyl)amino)(phenyl)methylene)-2-oxoindoline-6-carboxylate N-methyl-2-(4-methylpiperazin-1-yl)-N-(4-nitrophenyl)acetamide Nintedanib Impurity 76 N-Methyl-4-nitroaniline Nintedanib Impurity 67 Nintedanib Impurity 107 1,2-dichloro-4-(dichloromethyl)benzene BIBF 1202 Nintedanib Impurity 62 Ethanesulfonic acid isopropyl ester Methyl oxindole-5-carboxylate Nintedanib Impurity 52 2-Oxo-2,3-dihydro-1H-indole-6-carboxylic acid ethyl ester 2-Propanesulfonic acid sodium salt mon& 1-Acetyl-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acid methyl ester alpha,alpha,2,4-Tetrachlorotoluene Anisaldehyde Dimethyl Acetal