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3-hydroxy-2,4-dimethoxybenzaldehyde is a chemical compound characterized by the molecular formula C10H12O4. It is a white crystalline solid that is soluble in most organic solvents. 3-hydroxy-2,4-dimethoxybenzaldehyde has garnered attention in the scientific community due to its potential pharmacological properties, including antioxidant and anti-inflammatory effects, as well as its potential application in the development of new drugs and pharmaceutical products.

32246-34-7

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32246-34-7 Usage

Uses

Used in Organic Synthesis:
3-hydroxy-2,4-dimethoxybenzaldehyde is utilized as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for versatile reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Chemical Research:
In the field of chemical research, 3-hydroxy-2,4-dimethoxybenzaldehyde serves as a subject of study for understanding the properties and reactivity of similar compounds. Its behavior in different chemical environments provides insights into the development of new synthetic pathways and methodologies.
Used in Pharmaceutical Development:
3-hydroxy-2,4-dimethoxybenzaldehyde is used as a starting material or a building block in the development of new pharmaceutical products. Its potential pharmacological properties, such as antioxidant and anti-inflammatory effects, make it a promising candidate for the creation of novel drugs to address various health conditions.
Used in Antioxidant and Anti-inflammatory Applications:
Due to its inherent antioxidant and anti-inflammatory properties, 3-hydroxy-2,4-dimethoxybenzaldehyde is employed in the development of treatments and therapies aimed at combating oxidative stress and inflammation-related disorders. Its potential to mitigate these conditions makes it a valuable asset in the pharmaceutical and healthcare industries.

Check Digit Verification of cas no

The CAS Registry Mumber 32246-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,4 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32246-34:
(7*3)+(6*2)+(5*2)+(4*4)+(3*6)+(2*3)+(1*4)=87
87 % 10 = 7
So 32246-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O4/c1-12-7-4-3-6(5-10)9(13-2)8(7)11/h3-5,11H,1-2H3

32246-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2,4-dimethoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names EINECS 250-970-6

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:32246-34-7 SDS

32246-34-7Relevant academic research and scientific papers

SUBSTITUTED CHROMEN-4-ONE FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

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Page/Page column 31, (2020/07/31)

The present invention provides novel compounds having the general formula: (I) wherein R1 to R10, Gi, G2 and m are as described herein, compositions including the impounds and methods of using the compounds for the treatment of hepatitis B.

Synthetic methods for phoyunbenes A-D and thunalbene

-

, (2017/04/13)

Invented is a method for synthesizing thunalbene and phoyunbenes A-D via a Horner-Wadsworth-Emmons (HWE) reaction in a simple and effective way. The compounds of the present invention have shown anti-inflammatory effects in RAW-264.7 macrophage which is induced by lipopolysaccharide.

Syntheses of phoyunbenes A-D and thunalbene for their anti-inflammatory evaluation

Moon, Insu,Kim, Jin-Kyung,Jun, Jong-Gab

, p. 2907 - 2914 (2016/01/25)

Simple and efficient first syntheses of phoyunbenes A-D and thunalbene have been developed using Horner- Wadsworth-Emmons reaction as a key step. Later, their anti-inflammatory effects were investigated in lipopolysaccharide-induced RAW-264.7 macrophages. The results revealed that phoyunbenes A-D and thunalbene showed weak inhibitory activities without cytotoxicity on the production of nitric oxide (NO) which is an important inflammatory mediator.

Isolation, Structure, and Synthesis of Combretastatin C-1

Singh, Sheo Bux,Pettit, George R.

, p. 4105 - 4114 (2007/10/02)

A new cell growth inhibitory (PS ED50 2.2 μg/mL) phenanthraquinone designated combretastatin C-1 (2) has been isolated from the African tree Combretum caffrum.The structure (2) assigned combretastatin C-1 was based on high-resolution mass and NMR spectral analyses and confirmed by total syntheses.Synthetic routes 5b -> 6b -> 2 and especially 5c -> 6c -> 2 proved to be quite practical.

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