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p-Anisidine

ALDRICH/A88255 - 99%

Synonym: 4-Aminoanisole; 4-Methoxyaniline

CAS Number: 104-94-9
Empirical Formula (Hill Notation): C7H9NO
Molecular Weight: 123.15
MDL Number: MFCD00007864
Linear Formula: CH3OC6H4NH2
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-A88255-5G 5 g
 $23.50
1/EA		 Add To Favorites
45-A88255-100G 100 g
 $31.30
1/EA		 Add To Favorites
45-A88255-250G 250 g
 $63.40
1/EA		 Add To Favorites
45-A88255-1KG 1 kg
 $166.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: A88255-1KG
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: A88255-250G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: A88255-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: A88255-5G

 

assay 99%
autoignition temp. 959 °F
bp 240-243 °C (lit.)
form solid
InChI 1S/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3
InChI key BHAAPTBBJKJZER-UHFFFAOYSA-N
mp 56-59 °C (lit.)
Quality Level 200 
SMILES string COc1ccc(N)cc1
Application: p-Anisidine can undergo aerobic oxidation in the presence of gold catalysts to form aromatic azo compounds.
p-Anisidine can be used:
•  In the diastereoselective and enantioselective synthesis of CF3-substituted azoridines catalyzed by a chiral Bronsted acid.
•  To prepare 4-organoselenium-quinolines through multi-component Povarov reaction with ethyl glyoxylate and ethynyl(phenyl)selane, catalyzed by Yb(OTf)3.
•  As a starting material to synthesize 3-fluoro-6-methoxyquinoline in two steps.,
•  To prepare N-PMP protected α-aminopropargylphosphonates by reacting with terminal alkynes and diethyl formylphosphonate hydrate using silver(I) triflate as a catalyst.
Packaging: 1 kg in glass bottle
Packaging: 5, 100, 250 g in glass bottle
Purity 99%
bp 240-243 °C (lit.)
mp 56-59 °C (lit.)
UNSPSC 12352100

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