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Product Details
Uses |
4-Hydroxy-3-methylbenzaldehyde was used in the preparation of a new series of benzothiazole schiff bases which display antitumor activity against cervical cancer. Also used in the synthesis of novel pyrimidine derivatives which possess antibacterial properties against gram-positive and gram-negative bacteria. |
InChI:InChI=1/C8H8O2/c1-6-4-7(5-9)2-3-8(6)10/h2-5,10H,1H3
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chloroform
ortho-cresol
4-hydroxy-3-methyl-benzaldehyde
Conditions | Yield |
---|---|
chloroform; ortho-cresol; With sodium hydroxide; In water; at 60 ℃; for 6.5h;
With hydrogenchloride; In water;
|
65% |
With sodium hydroxide; In water; at 60 ℃; for 7h;
|
65% |
With sodium hydroxide; β‐cyclodextrin; In water; at 60 ℃; for 8h;
|
11% |
3-methyl-4-anisaldehyde
4-hydroxy-3-methyl-benzaldehyde
Conditions | Yield |
---|---|
With boron tribromide; In dichloromethane; for 21h; Ambient temperature;
|
87% |
3-methyl-4-anisaldehyde; With boron tribromide; In dichloromethane; at 0 - 20 ℃; for 50h;
In methanol; at 15 ℃; for 0.5h; Heating / reflux;
In methanol; water; for 0.5h;
|
70% |
4-Amino-3-methylbenzaldehyde
formaldehyd
ortho-cresol
hydrogen cyanide
4-hydroxy-3-methoxy-5-(phenyldiazenyl)benzaldehyde
(4-hydroxy-5-isopropyl-2-methyl-phenyl)-(4-hydroxy-3-methyl-phenyl)-acetonitrile
4-hydroxy-3-methylbenzoic acid
4t-(4-hydroxy-3-methyl-phenyl)-but-3-en-2-one
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