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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide

5-ACETAMIDOSALICYALDEHYDE synthesis

5synthesis methods
90-02-8 Synthesis
Salicylaldehyde

90-02-8
445 suppliers
$9.00/1g

75-05-8 Synthesis
Acetonitrile

75-05-8
966 suppliers
$10.00/10g

5-ACETAMIDOSALICYALDEHYDE

16358-44-4
2 suppliers
inquiry

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Yield:16358-44-4 81%

Reaction Conditions:

with tetra-n-butylammonium hexafluoridophosphate at 20; for 5 h;Electrolysis;Green chemistry;regioselective reaction;Ritter Amidation;

References:

Taily, Irshad Maajid;Saha, Debarshi;Banerjee, Prabal [Organic Letters,2022,vol. 24,# 12,p. 2310 - 2314] Location in patent:supporting information

103-90-2 Synthesis
Acetaminophen

103-90-2
1046 suppliers
$9.00/1g

76-05-1 Synthesis
Trifluoroacetic acid

76-05-1
677 suppliers
$9.00/1g

5-ACETAMIDOSALICYALDEHYDE

16358-44-4
2 suppliers
inquiry

References
50-00-0 Synthesis
Formaldehyde

50-00-0
843 suppliers
$10.00/25g

103-90-2 Synthesis
Acetaminophen

103-90-2
1046 suppliers
$9.00/1g

5-ACETAMIDOSALICYALDEHYDE

16358-44-4
2 suppliers
inquiry

References
Hexamethylenetetramine

100-97-0
7 suppliers
$14.00/250G

103-90-2 Synthesis
Acetaminophen

103-90-2
1046 suppliers
$9.00/1g

5-ACETAMIDOSALICYALDEHYDE

16358-44-4
2 suppliers
inquiry

References
Methanediol,1-[2-(acetyloxy)-5-nitrophenyl]-, 1,1-diacetate

24590-01-0
0 suppliers
inquiry

5-ACETAMIDOSALICYALDEHYDE

16358-44-4
2 suppliers
inquiry

References