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2H-Pyran-2-one, 4-methoxy-6-[2-(4-methoxyphenyl)ethyl]- is a complex organic compound with the molecular formula C16H18O5. It is a derivative of 2H-pyran-2-one, featuring a 4-methoxy group and a 2-(4-methoxyphenyl)ethyl substituent at the 6-position. 2H-Pyran-2-one, 4-methoxy-6-[2-(4-methoxyphenyl)ethyl]- is characterized by its unique structure, which includes a pyranone ring system with oxygen-containing functional groups. It is synthesized through various chemical reactions and is used in the pharmaceutical and chemical industries for the development of drugs and other organic compounds. The compound's properties, such as its solubility and reactivity, are influenced by the presence of the methoxy groups and the ethyl linker, making it a versatile building block in organic synthesis.

3155-52-0

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3155-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3155-52-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3155-52:
(6*3)+(5*1)+(4*5)+(3*5)+(2*5)+(1*2)=70
70 % 10 = 0
So 3155-52-0 is a valid CAS Registry Number.

3155-52-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-6-[2-(4-methoxyphenyl)ethyl]pyran-2-one

1.2 Other means of identification

Product number -
Other names dihydroyangonin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3155-52-0 SDS

3155-52-0Downstream Products

3155-52-0Relevant academic research and scientific papers

Heck-matsuda arylation as a strategy to access kavalactones isolated from polygala sabulosa, piper methysticum, and analogues

Soldi, Cristian,Moro, Angelica V.,Pizzolatti, Moacir G.,Correia, Carlos R. D.

, p. 3607 - 3616 (2012/07/31)

Herein, we describe the total syntheses of three bioactive pyrones isolated from Polygala sabulosa (i.e., 1, 4, and 7) and eight isolated from Piper methysticum (i.e., 8-10, 13, 15, and 18-20) using the Heck-Matsuda arylation as the key strategy. The evaluation of this methodology by employing different arenediazonium tetrafluoroborates revealed that the Heck arylation was more efficient when the olefin undergoing arylation possessed the vinyl-2-pyrone structural unit instead of the vinyl dihydro-2-pyrone moiety. The Heck-Matsuda arylation of many of the examined olefins proceeded in a practical manner with total regio- and stereocontrol.

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