81805-98-3

Usage

Uses

Used in Pharmaceutical Industry:
7-HYDROXY-1,3-BENZODIOXOLE-5-CARBOXALDEHYDE is used as a protective agent for its ability to shield cells against oxidative damage and the aging process, making it valuable in the development of medications aimed at promoting health and longevity.
Used in Cosmetic Industry:
In the cosmetic sector, 7-HYDROXY-1,3-BENZODIOXOLE-5-CARBOXALDEHYDE is utilized as an ingredient to protect the skin from oxidative stress, thereby contributing to anti-aging formulations and skincare products.
Used in Food Industry:
7-HYDROXY-1,3-BENZODIOXOLE-5-CARBOXALDEHYDE is employed as a flavoring agent, leveraging its unique properties to enhance the taste profiles of various food products.
Used in Perfume Industry:
7-HYDROXY-1,3-BENZODIOXOLE-5-CARBOXALDEHYDE is also used as a fragrance in the perfume industry, where its distinct scent characteristics contribute to the creation of various olfactory compositions.
Used in Health Research:
7-HYDROXY-1,3-BENZODIOXOLE-5-CARBOXALDEHYDE is studied for its potential therapeutic effects on health conditions such as cancer and neurodegenerative diseases, indicating its possible use as a therapeutic agent in future medical treatments.

InChI:InChI=1/C8H6O4/c9-3-5-1-6(10)8-7(2-5)11-4-12-8/h1-3,10H,4H2

Upstream product

• 19522-96-4 7-bromo-benzo[1,3]dioxole-5-carbaldehyde 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 16414-34-9 3-bromo-4,5-dihydroxybenzaldehyde 
• 81805-94-9 3-bromo-N-cyclohexyl-4,5-methylenedioxybenzylideneimine 

Downstream Products

• 795278-08-9 6-bromo-7-hydroxybenzo[d][1,3]dioxole-5-carbaldehyde 
• 1037620-82-8 3-[2H₃]methoxy-4,5-(methylenedioxy)benzaldehyde 
• 795278-07-8 6-bromo-7-methoxybenzo[d][1,3] dioxole-5-carbaldehyde 
• 181701-06-4 interiotherin A 
• 852123-16-1 ((1S,2S,3S)-4-(4-(benzyloxy)benzo[d][1,3]dioxol-6-yl)-1-(5-bromo-4-methoxybenzo[d][1,3]dioxol-6-yl)-2,3-dimethylbutoxy)(tert-butyl)dimethylsilane 
• 852123-20-7 ((1S,2S,3S)-4-(5-bromo-4-hydroxybenzo[d][1,3]dioxol-6-yl)-1-(5-bromo-4-methoxybenzo[d][1,3]dioxol-6-yl)-2,3-dimethylbutoxy)(tert-butyl)dimethylsilane 
• 852123-22-9 ((1S,2S,3S)-1,4-bis(5-bromo-4-methoxybenzo[d][1,3]dioxol-6-yl)-2,3-dimethylbutoxy)(tert-butyl)dimethylsilane 
• 852123-25-2 ((1S,2S,3S)-1-(5-bromo-4-methoxybenzo[d][1,3]dioxol-6-yl)-4-(4-methoxybenzo[d][1,3]dioxol-6-yl)-2,3-dimethylbutoxy)(tert-butyl)dimethylsilane 
• 852123-18-3 ((1S,2S,3S)-4-(4-hydroxybenzo[d][1,3]dioxol-6-yl)-1-(5-bromo-4-methoxybenzo[d][1,3]dioxol-6-yl)-2,3-dimethylbutoxy)(tert-butyl)dimethylsilane 
• 852123-14-9 ((1S,2S)-1-(5-bromo-4-methoxybenzo[d][1,3]dioxol-6-yl)-2,3-dimethylbut-3-enyloxy)(tert-butyl)dimethylsilane 
• 852123-12-7 (1S,2S)-1-(5-bromo-4-methoxybenzo[d][1,3]dioxol-6-yl)-2,3-dimethylbut-3-en-1-ol 

Relevant academic research and scientific papers

Synthesis of deuterium-labelled standards of (±)-DOM and (±)-MMDA

This study describes the synthesis of deuterium-labelled (±)-4-methyl-2,5-dimethoxyamphetamine (DOM) and (+)-l-(7-methoxy-l,3- benzodioxol-5-yl)propan-2-amine (MMDA). The isotopically labelled compounds are potentially used as internal standards in gas chromatography-mass spectrometry (GC-MS) assays. Copyright

Aromatic Hydroxylation. Hydroxybenzaldehydes from Bromobenzaldehydes via Reaction of in Situ Generated, Lithiated α-Morpholinobenzyl Alkoxides with Nitrobenzene

A general method for the one-step conversion of bromobenzaldehydes to the corresponding hydroxybenzaldehydes has been developed.The method involves in situ protection of the aldehyde function of the bromobenzaldehyde as its lithium morpholinoalkoxide, followed by lithium-bromine exchange, reaction with nitrobenzene at -75 deg C, and a subsequent acidic workup.The method has been applied to the synthesis of 4,5-dimethoxy-3-hydroxy- (1a), 3,5-dimethoxy-2-hydroxy- (2a), 3,5-bis(benzyloxy)-2-hydroxy- (2b), 3,4-dimethoxy-2-hydroxy- (14), 3-hydroxy-4,5-(methylenedioxy)- (16), and 4,5-dimethoxy-2-hydroxybenzaldehydes (18) from the bromobenzaldehydes 4, 12a, 12b, 13, 15, and 17, respectively.