Methyl 4-(chlorocarbonyl)benzoate

CAS: 7377-26-6

Ref. 3D-FM31274

Información del producto

• Nombre: Methyl 4-(chlorocarbonyl)benzoate
• Sinónimos: 4-Chlorocarbonylbenzoic acid methyl esterMethyl terephthaloyl chlorideMethyl 4-(chloroformyl)benzoate, 1-(Chloroformyl)-4-(methoxycarbonyl)benzene, 4-(Carbomethoxy)benzoyl chloride, 4-(Chlorocarbonyl)-Benzoic Acid Methyl Ester, 4-(Chloroformyl)benzoic acid methyl ester, 4-(Methoxycarbonyl)benzoyl chloride, 4-Chlorocarbonylbenzoic acid methyl ester, Benzoic acid, 4-(chlorocarbonyl)-, methyl ester, Benzoic acid, p-(chloroformyl)-, methyl ester, Methyl 4-(carbonochloridoyl)benzoate, Methyl 4-(chlorocarbonyl)benzote, Methyl 4-(chloroformyl)benzoate, Methyl 4-carboxybenzoyl chloride, Methyl 4-chlorocarbonylbenzoate, Methyl p-(chlorocarbonyl)benzoate, Methyl p-(chloroformyl)benzoate, Methyl terephthalic chloride, Methyl terephthaloyl chloride, Methyl terephthalyl chloride, Monomethyl terephthalate acid chloride, Monomethyl terephthaloyl chloride, Terephthalic acid chloride monomethyl ester, Terephthalic acid monomethyl ester chloride, Terephthaloyl chloride methyl ester, p-(Carbomethoxy)benzoyl chloride, p-(Methoxycarbonyl)benzoyl chloride
• CAS: 7377-26-6

Descripción

Methyl 4-(chlorocarbonyl)benzoate is a synthetic retinoid that has potent inhibitory activity against the growth factor-stimulated proliferation of human HL-60 cells. It interacts with the cholesterol ester transfer protein, which inhibits the synthesis of prostaglandins and thromboxanes, resulting in an anti-inflammatory effect. Methyl 4-(chlorocarbonyl)benzoate has been shown to be effective in inhibiting the growth of cancer cells by light emission. This compound also exhibits high hydrogen bonding interactions with pyridinium ions and quinolinium ions.

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 198.6 g/mol
• Fórmula: C₉H₇ClO₃
• Pureza: Min. 95%
• InChI: InChI=1S/C9H7ClO3/c1-13-9(12)7-4-2-6(3-5-7)8(10)11/h2-5H,1H3
• Clave InChI: InChIKey=CVXXHXPNTZBZEL-UHFFFAOYSA-N
• SMILES: COC(=O)c1ccc(C(=O)Cl)cc1