131-12-4

Basic information

• Product Name: pimpinellin
• Synonyms: 5,6-Dimethoxy-2H-furo[2,3-h]-1-benzopyran-2-one;Pimpinecilin;5,6-dimethoxyfuro[2,3-h]chromen-2-one;5,6-DiMethoxy-2H-furo[2,3-h]chroMen-2-one
• CAS NO: 131-12-4
• Molecular Formula: C13H10O5
• Molecular Weight: 246.21
• Mol File: 131-12-4.mol

Chemical Properties

• Melting Point: 119°
• Boiling Point: 441 °C at 760 mmHg
• Flash Point: 220.5 °C
• Appearance: /
• Density: 1.352 g/cm³
• Vapor Pressure: 5.62E-08mmHg at 25°C
• Refractive Index: 1.611
• Storage Temp.: 2-8°C
• CAS DataBase Reference: pimpinellin(CAS DataBase Reference)
• NIST Chemistry Reference: pimpinellin(131-12-4)
• EPA Substance Registry System: pimpinellin(131-12-4)

Safety Data

• Hazardous Substances Data: 131-12-4(Hazardous Substances Data)

Usage

Uses

GABA receptor antagonist, phototoxin

InChI:InChI=1/C13H10O5/c1-15-11-7-3-4-9(14)18-10(7)8-5-6-17-12(8)13(11)16-2/h3-6H,1-2H3

Upstream product

• 24099-30-7 6-hydroxy-5-methoxyangelicin 
• 74-88-4 methyl iodide 
• 61265-07-4 heratomol 
• 77-78-1 dimethyl sulfate 
• 250639-95-3 6-benzyloxy-furo[2,3-h]chromen-2-one 
• 115591-55-4 5-ethynyl-4,6,7-trimethoxybenzofuran 
• 115591-57-6 6-methoxy-5-<2-(methoxycarbonyl)-1-ethynyl>-4,7-benzofuranquinone 
• 115591-53-2 4,6,7-trimethoxy-5-<2-(trimethylsilyl)-1-ethynyl>benzofuran 
• 115591-56-5 5-<2-(methoxycarbonyl)-1-ethynyl>-4,6,7-trimethoxybenzofuran 

Relevant articles and documents

Total syntheses of the coumarin-containing natural products pimpinellin and fraxetin using Au(I)-catalyzed intramolecular hydroarylation (IMHA) chemistry

The title natural products (1 and 2, respectively) have been synthesized by Au(I)-catalyzed intramolecular hydroarylation (IMHA) of the relevant aryl propiolate esters (e.g., 13), which were themselves formed by reaction of the corresponding phenols with either 3-(trimethylsilyl)propiolic acid or propiolic acid and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride or dicyclohexylcarbodiimide. (±)-Purpurasol (3) was readily derived from fraxetin (2) by established procedures.

Synthesis and antifungal activity of coumarins and angular furanocoumarins

Angelicin, a naturally occurring furanocoumarin, that showed antifungal activity, was considered as a lead structure for a group of synthetic coumarins. Antifungal activities of the synthesized coumarins and angelicin derivatives were reported against Can

Efficient Synthesis of Furochromone and Furocoumarin Natural Products (Khellin, Pimpinellin, Isophellopterin) by Thermal Rearrangement of 4-Furyl-4-hydroxycyclobutenones

Diethyl squarate was converted in three steps to a highly functionalized benzofuran 6b, which served as an intermediate in a high yield synthesis of khellinone (9), a versatile precursor to a variety of linear furochromones, including the natural product khellin.The use of dimethyl squarate gave a similar benzofuran intermediate 6a, which was used in the first total syntheses of the furocoumarins pimpinellin (14) and isophellopterin (15).The key benzofuran intermediates were prepared by thermal rearrangement of (trimethylsilyl)ethynyl-substituted 4-furanyl-4-hydroxycyclobutenones 2a,b.The alkynyl moiety of 6b was readily converted to the acetyl group of khellinone by mercury-catalyzed hydrolysis.Alternatively, the TMS protecting group in 6a was removed, and the lithium acetylide was treated with methyl chloroformate.The resulting trimethoxybenzofuran was treated with CAN to generate the quinone.Catalytic hydrogenation gave reduction of the quinone to the hydroquinone and alkyne to the cis-alkene.Simultaneous lactonization gave the desired coumarin 13.Methylation of this at the phenolic site gave pimpinellin (14).The same phenol was prenylated to give isophellopterin (15).Finally, oxidation of the phenol with CAN gave a previously unknown orthoquinone, (16), and angular isomer of psoralenquinone.