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6-(3,4,5-trimethoxybenzoyl)-1,3-benzodioxole-5-carboxylic acid is a complex organic compound with the molecular formula C18H17O9. It is characterized by a benzodioxole ring, which is a benzene ring with two oxygen atoms forming a cyclic ether structure. The compound features a 3,4,5-trimethoxybenzoyl group attached to the 6-position of the benzodioxole, which means that the benzoic acid has three methoxy groups (-OCH3) attached to the 3rd, 4th, and 5th carbon atoms. Additionally, it has a carboxylic acid group (-COOH) at the 5-position of the benzodioxole ring. This chemical is known for its potential applications in pharmaceuticals and as a synthetic intermediate in the preparation of various biologically active compounds. Its structure provides a unique set of properties that can be exploited in the design of new drugs and other chemical products.

7470-99-7

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7470-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7470-99-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7470-99:
(6*7)+(5*4)+(4*7)+(3*0)+(2*9)+(1*9)=117
117 % 10 = 7
So 7470-99-7 is a valid CAS Registry Number.

7470-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(3,4,5-trimethoxybenzoyl)-1,3-benzodioxole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4,5-Methylendioxy-2-(3,4,5-trimethoxy-benzoyl)-benzoesaeure

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:7470-99-7 SDS

7470-99-7Relevant academic research and scientific papers

BIOSYNTHESIS OF PODOPHYLLUM LIGNANS - I. CINNAMIC ACID PRECURSORS OF PODOPHYLLOTOXIN IN PODOPHYLLUM HEXANDRUM

Jackson, David E.,Dewick, Paul M.

, p. 1029 - 1036 (2007/10/02)

Feeding experiments in Podophyllum hexandrum plants have established that phenylalanine, cinnamic acid and ferulic acid are good precursors of the two major aryltetralin lignans podophyllotoxin and 4'-demethylpodophyllotoxin.Sinapic and 3,4,5-trimethoxycinnamic acids were poorly utilized, showing that the substitution pattern of the pendent aryl ring is built up after coupling of the two phenylpropane units.Degradation studies on podophyllotoxin derived from ferulic acid show that the two halves of the lignan molecule are equally labelled supporting a biosynthetic sequence involving oxidative coupling of two similar phenylpropane precursors having the substitution pattern of ferulic acid.Although 3,4-methylenedioxycinnamic acid was readily incorporated, degradative studies prove that this compound is not incorporated intact, but via a metabolic sequence in which the methylenedioxy carbon atom enters the C1-pool and then labels the methylenedioxy and methoxyl substituents of podophyllotoxin.The rest of the skeleton is incorporated via ferulic acid, presumably by way of caffeic acid.Key Word Index - Podophyllum hexandrum; Podophyllaceae; aryltetralin; lignans; biosynthesis; podophyllotoxin.

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