p-(Dimethoxymethyl)anisol

P-ANISALDEHYDE DIMETHYL ACETAL Struktur
2186-92-7
CAS-Nr.
2186-92-7
Bezeichnung:
p-(Dimethoxymethyl)anisol
Englisch Name:
P-ANISALDEHYDE DIMETHYL ACETAL
Synonyma:
-4-methoxybenzene;ANISIC ALDEHYDE DMA;1-(Dimethoxymethyl);Nintedanib Impurity 33;α,α,4-Trimethoxytoluene;Anisaldehyddimethylacetal;p-(dimethoxymethyl)anisole;4-(Dimethoxymethyl)anisole;ANISALDEHYDE DIMETHYL ACETAL;Anisicaldehydedimethylacetal
CBNumber:
CB7140121
Summenformel:
C10H14O3
Molgewicht:
182.22
MOL-Datei:
2186-92-7.mol

p-(Dimethoxymethyl)anisol Eigenschaften

Siedepunkt:
85-87 °C0.1 mm Hg(lit.)
Dichte
1.07 g/mL at 20 °C(lit.)
Dampfdruck
2.407-48Pa at 25-61.2℃
Brechungsindex
n20/D 1.505
Flammpunkt:
97°C
storage temp. 
2-8°C
Löslichkeit
H2O: soluble
Aggregatzustand
Liquid
Farbe
Clear colorless to light yellow
Geruch (Odor)
at 100.00 %. mild floral hawthorn jasmin lilac elderflower
Geruchsart
floral
Wasserlöslichkeit
Miscible with alcohol and many organic solvents. Slightly miscible with water.
BRN 
2048930
LogP
2 at 25℃
CAS Datenbank
2186-92-7(CAS DataBase Reference)
EPA chemische Informationen
p-(Dimethoxymethyl)anisole (2186-92-7)

Sicherheit

S-Sätze: 24/25
WGK Germany  1
10
TSCA  Yes
HS Code  29110000

p-(Dimethoxymethyl)anisol Chemische Eigenschaften,Einsatz,Produktion Methoden

S-Sätze Betriebsanweisung:

S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

clear colorless to light yellow liquid

Verwenden

4-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.

p-(Dimethoxymethyl)anisol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


p-(Dimethoxymethyl)anisol Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 264)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Suzhou BEC Biological Technology Co., Ltd.
+undefined13771885869
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Capot Chemical Co.,Ltd.
571-85586718 +8613336195806
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8485655694
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+8618530059196
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Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671
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WinWin Chemical CO., Limited
+86-0086-577-64498589 +86-15355981851
sales@win-winchemical.com China 13854 58

2186-92-7(p-(Dimethoxymethyl)anisol)Verwandte Suche:


  • 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
  • Benzene, 1-(dimethoxymethyl)-4-methoxy-
  • Anisaldehyddimethylacetal
  • 4-Methoxybenzaldehyde dimethyl acetal, 98+%
  • alpha,alpha,4-Trimethoxytoluene
  • 4-Methoxybenzaldehyde dimethyl acetal, α,α,4-Trimethoxytoluene
  • 1-Methoxy-4-(dimethoxymethyl)benzene
  • 4-(Dimethoxymethyl)anisole
  • p-Anisaldehyde dimethyl acetal,98%
  • p-Anisaldehyde Dimethyl Acetalp-Anisaldehyde Dimethyl Acetal
  • α,α,4-Trimethoxytoluene
  • p-Anisaldehyde diethyl acetal
  • p-Anisaldehyde diMethyl acetal, 98% 25GR
  • 4-Methoxybenzaldehyde Dimethyl Acetal alpha,alpha,4-Trimethoxytoluene
  • AnisaldehydediMethyl acetaltwo
  • Anisaldehyde dimethyl acetal >=98.5% (GC)
  • 1-(Dimethoxymethyl)
  • -4-methoxybenzene
  • 4-chlorobenzoic acid [5-chloro-3-[(4-chlorophenyl)-oxomethoxy]-2-oxolanyl]methyl ester
  • Nintedanib Impurity 33
  • 4-Methoxybenzaldehyde dimethyl acetal (Anisaldehyde dimethyl acetal)
  • p-Anisaldehyde Dimethyl Acetal >
  • para-anisaldehyde dimethyl acetal
  • p-Methoxybenzaldehyde dimethylacetal
  • 2186-92-7
  • Building Blocks
  • Reagents for Oligosaccharide Synthesis
  • Organic Building Blocks
  • Acetals/Ketals/Ortho Esters
  • Oxygen Compounds
  • Biochemistry
  • Reagents for Oligosaccharide Synthesis
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