A88255
p-Anisidine
99%
Synonyme(s) :
4-Aminoanisole, 4-Methoxyaniline
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A propos de cet article
Formule linéaire :
CH3OC6H4NH2
Numéro CAS:
Poids moléculaire :
123.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
471556
Assay:
99%
Form:
solid
Service technique
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assay
99%
form
solid
autoignition temp.
959 °F
bp
240-243 °C (lit.)
mp
56-59 °C (lit.)
SMILES string
COc1ccc(N)cc1
InChI
1S/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3
InChI key
BHAAPTBBJKJZER-UHFFFAOYSA-N
Application
p-Anisidine can undergo aerobic oxidation in the presence of gold catalysts to form aromatic azo compounds.
p-Anisidine can be used:
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.
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Danger
Classe de stockage
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
flash_point_f
251.6 °F - closed cup
flash_point_c
122 °C - closed cup
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Carc. 1B - STOT RE 2
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