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Anisaldehyde dimethyl acetal - 97%, high purity , CAS No.2186-92-7

  • ≥97%
Item Number
A111315
Grouped product items
SKUSizeAvailabilityPrice Qty
A111315-5ml
5ml
In stock
$14.90
A111315-25ml
25ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$49.90
A111315-50ml
50ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$75.90
A111315-100ml
100ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$120.90
A111315-250ml
250ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$241.90
A111315-500ml
500ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$386.90
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Aromatic Ring Compounds ketone Non heterocyclic block

Basic Description

Synonyms2186-92-7|1-(Dimethoxymethyl)-4-methoxybenzene|p-Anisaldehyde dimethyl acetal|Anisaldehyde dimethyl acetal|p-(Dimethoxymethyl)anisole|4-Methoxybenzaldehyde dimethyl acetal|Benzene, 1-(dimethoxymethyl)-4-methoxy-|Anisicaldehyde dimethylacetal|p-anisaldehyd
Specifications & Purity97%
Storage TempStore at 2-8°C,Argon charged
Shipped InWet ice
Product Description

Anisaldehyde dimethyl acetal is a clear, colorless to light yellow liquid. The flash point for anisaldehyde dimethyl acetal is 114.0°C. It undergoes allylation reactions with allyltrimethylsilane catalysed by Iron(III) chloride[1]. Anisaldehyde dimethyl acetal undergoes ytterbium-catalyzed tandem carboalkoxylation/Friedel–Crafts reaction with 1-phenylbenzylidenecyclopropane to yield 1-(p-anisyl)-2-(2-methoxyethyl)-3-phenylindene.

Names and Identifiers

Pubchem Sid488185043
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488185043
IUPAC Name 1-(dimethoxymethyl)-4-methoxybenzene
INCHI InChI=1S/C10H14O3/c1-11-9-6-4-8(5-7-9)10(12-2)13-3/h4-7,10H,1-3H3
InChi Key NNHYAHOTXLASEA-UHFFFAOYSA-N
Canonical SMILES COC1=CC=C(C=C1)C(OC)OC
Isomeric SMILES COC1=CC=C(C=C1)C(OC)OC
WGK Germany 1
PubChem CID 75140
Molecular Weight 182.22
Beilstein 2048930
Reaxy-Rn 2048930

Certificates

Certificate of Analysis(COA)

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13 results found

Lot NumberCertificate TypeDateItem
J2213025Certificate of AnalysisJul 19, 2024 A111315
J2213026Certificate of AnalysisJul 19, 2024 A111315
H2409029Certificate of AnalysisJul 18, 2024 A111315
H2409030Certificate of AnalysisJul 18, 2024 A111315
H2409031Certificate of AnalysisJul 18, 2024 A111315
H2409032Certificate of AnalysisJul 18, 2024 A111315
H2204197Certificate of AnalysisMay 21, 2024 A111315
K2110752Certificate of AnalysisAug 02, 2023 A111315
F2104092Certificate of AnalysisMar 10, 2023 A111315
B2325254Certificate of AnalysisMar 03, 2023 A111315
J2213023Certificate of AnalysisAug 19, 2022 A111315
K2303071Certificate of AnalysisAug 19, 2022 A111315
H2204198Certificate of AnalysisMay 08, 2021 A111315

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Chemical and Physical Properties

SolubilityMiscible with alcohol and many organic solvents. Slightly miscible with water.
SensitivityMoisture sensitive
Refractive Index1.505
Flash Point(°F)237.2 °F
Flash Point(°C)98 °C
Boil Point(°C)253°C

Safety and Hazards(GHS)

WGK Germany 1
Reaxy-Rn 2048930

Related Documents

 SDS

 Specification Sheet

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References

1. P K Chan,M Aldrich,R G Cook,H Busch.  (1986-02-05)  Amino acid sequence of protein B23 phosphorylation site..  The Journal of biological chemistry,  261  ((4)): (1868-1872).  [PMID:3944116]
2. Hansruedi Stettler,Gregor Suri,Martin Spiess.  (2005-04-06)  Proprotein convertase PC3 is not a transmembrane protein..  Biochemistry,  44  ((14)): (5339-5345).  [PMID:15807527]
3. Yasumasa Hara,Midori A Arai,Kanae Sakai,Naoki Ishikawa,Tohru Gonoi,Takashi Yaguchi,Masami Ishibashi.  (2017-12-07)  Dehydropropylpantothenamide isolated by a co-culture of Nocardia tenerifensis IFM 10554.  Journal of natural medicines,  72  ((1)): (280-289).  [PMID:29209902]

Solution Calculators

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