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13063-09-7

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13063-09-7 Usage

General Description

2,4,6-Trimethoxycinnamic acid is a chemical compound with the molecular formula C12H14O5. It belongs to the group of cinnamic acid derivatives and is commonly found in plant sources such as cloves and Glinus oppositifolius. 2,4,6-TRIMETHOXYCINNAMIC ACID has been studied for its potential biological and pharmacological properties, including antioxidant, anti-inflammatory, and potential anticancer activities. It has also been investigated for its role in the synthesis of natural products and as a potential precursor for the development of new pharmaceuticals. Overall, 2,4,6-Trimethoxycinnamic acid is a compound of interest for its diverse range of potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 13063-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,6 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13063-09:
(7*1)+(6*3)+(5*0)+(4*6)+(3*3)+(2*0)+(1*9)=67
67 % 10 = 7
So 13063-09-7 is a valid CAS Registry Number.

13063-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-TRIMETHOXYCINNAMIC ACID

1.2 Other means of identification

Product number -
Other names 2,4,6-Trimethoxy-zimtsaeure

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:13063-09-7 SDS

13063-09-7Relevant articles and documents

Radical-Cation Vinylcyclopropane Rearrangements by TiO2Photocatalysis

Maeta, Naoya,Kamiya, Hidehiro,Okada, Yohei

supporting information, p. 6551 - 6566 (2020/07/14)

Radical cation vinylcyclopropane rearrangements by TiO2 photocatalysis in lithium perchlorate/nitromethane solution are described. The reactions are triggered by oxidative single electron transfer, which is followed by immediate ring-opening of the cyclopropanes to generate distonic radical cations as unique reactive intermediates. This approach can also be applied to vinylcyclobutane, leading to the construction of six-membered rings. A stepwise mechanism via distonic radical cations is proposed based on preliminary mechanistic studies, which is supported by density functional theory calculations.

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