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Molecular Formula: C9H8O3
Molecular Weight: 164.16
EINECS: 610-511-6
Purity: 97% Min.
Package: 5 g / 25 g / 1 kg / 25 kg
CAS: 501-98-4 trans-4-Hydroxycinnamic acid
trans-p-Coumaric Acid is the E-isomer of p-Coumaric Acid , a hydroxy derivative of Cinnamic Acid with antioxidant properties. p-Coumaric acid is a is a major component of lignocellulose. Studies suggest that p-Coumaric Acid may reduce the risk of cancer by reducing the formation of carcinogenic nitrosamines.
ITEMS | SPECIFICATION |
Melting point | 214 ¡ãC (dec.)(lit.) |
InChIKey | NGSWKAQJJWESNS-ZZXKWVIFSA-N |
storage temp. | Keep in dark place,Sealed in dry,Room Temperature |
solubility | ethanol |
Merck | 14,2560 |
color | Off-white to beige or greenish |
refractive index | 1.4500 |
form | Powder |
EPA Substance Registry System | 2-Propenoic acid, 3-(4-hydroxyphenyl)-, (2E)- (501-98-4) |
Water Solubility | soluble |
density | 1.1403 |
Boiling point | 231.61¡ã°ä&²Ô²ú²õ±è; |
pka | 4.65¡À0.10 |
NIST Chemistry Reference | p-Hydroxycinnamic acid(501-98-4) |
BRN | 2207383 |
CAS DataBase Reference | 501-98-4(CAS DataBase Reference) |
Production:
The preparation method uses acetylsalicylic chloride as raw material, reacts with diethyl malonate in acetonitrile solvent in the presence of magnesium chloride, adds triethylamine, and reacts at 0¡ãC for 1 hour to obtain (2-acetoxybenzene) The product of diethyl formyl)malonate is then heated to 50¡ãC in a potassium hydroxide/methanol solution, reacted for 3h, and cyclized to obtain the product. Ethyl acetoacetate can also be used as a raw material, in the presence of sodium hydroxide, in isobutyl methyl ketone solvent with acetylsalicylic chloride at 15-20 ¡æ for 3.5h to obtain 365betÓéÀÖbook to 2-(2-hydroxybenzoyl ) Sodium acetoacetate, the reaction product is reacted with hydrochloric acid at 25-30¡ãC for 30 minutes to obtain 3-acetyl-4-hydroxycoumarin, and then heated at 90-95¡ãC under concentrated sulfuric acid for 4 hours to obtain the product. You can also use 2-hydroxyacetophenone as a raw material, in the presence of potassium carbonate, pass 5.88MPa carbon dioxide into the autoclave, let it pass for 15h at room temperature, and then keep it at 60¡æ for 15h, firstly produce 2-hydroxybenzene-3- Oxypropionic acid, and then cyclic synthesis product.
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