241127-72-0

Basic information

• Product Name: Benzaldehyde, 2-bromo-3,6-dihydroxy- (9CI)
• Synonyms: Benzaldehyde, 2-bromo-3,6-dihydroxy- (9CI);2-Bromo-3,6-dihydroxybenzenecarbaldehyde;2-Bromo-3,6-dihydroxybenzaldehyde
• CAS NO: 241127-72-0
• Molecular Formula: C₇H₅BrO₃
• Molecular Weight: 217.0168
• Product Categories: ALCOHOL
• Mol File: 241127-72-0.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzaldehyde, 2-bromo-3,6-dihydroxy- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-bromo-3,6-dihydroxy- (9CI)(241127-72-0)
• EPA Substance Registry System: Benzaldehyde, 2-bromo-3,6-dihydroxy- (9CI)(241127-72-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 241127-72-0(Hazardous Substances Data)

Usage

General Description

Benzaldehyde, 2-bromo-3,6-dihydroxy- (9CI) is a chemical compound with the molecular formula C7H5BrO3. It is a derivative of benzaldehyde, a common building block in organic synthesis. The presence of the bromine and hydroxyl groups in this compound makes it useful for a variety of chemical reactions and processes, including pharmaceutical and agrochemical synthesis. It is also known for its sweet, almond-like aroma, making it a popular ingredient in the fragrance and flavoring industry. The compound is typically used as an intermediate in the production of various chemicals and is widely used in research and industrial applications.

Upstream product

• 93-02-7 2,5-dimethoxybenzaldehyde 
• 1194-98-5 2,5-Dihydroxybenzaldehyde 

Downstream Products

• 877319-66-9 2-bromo-6-hydroxy-3-methoxymethoxy-benzaldehyde 
• 341024-21-3 5-methoxy-2-phenylbenzofuran-4-carbaldehyde 
• 1448962-74-0 2-(2-fluorophenyl)-5-hydroxybenzofuran-4-carbaldehyde 
• 1448962-75-1 2-(2-fluorophenyl)-5-methoxybenzofuran-4-carbaldehyde 
• 1448962-77-3 C₂₃H₁₈O₄ 
• 1448962-71-7 1'-((5-methoxy-2-phenylbenzofuran-4-yl)methyl)-1,4'-bipiperidine 
• 1448962-78-4 1-((2-(2-benzyloxyphenyl)-5-methoxybenzofuran-4-yl)methyl)-N,N-dimethylpiperidin-4-amine 
• 58450-00-3 sydowinin B 
• 1379535-87-1 C₃₆H₅₂O₁₁Si 
• 1379535-86-0 2-((benzyloxy)methyl)-3-bromo-1,4-bis(methoxymethoxy)benzene 
• 1379535-84-8 C₁₅H₁₁NO₆ 
• 1379535-80-4 C₂₉H₄₁NO₁₀Si 
• 1379535-82-6 C₂₈H₄₁BrO₁₀Si 
• 1379535-81-5 C₂₈H₄₃BrO₁₀Si 

Relevant articles and documents

Asymmetric Total Syntheses and Structure Revisions of Eurotiumide A and Eurotiumide B, and Their Evaluation as Natural Fluorescent Probes

Asymmetric total syntheses and structure revisions of dihydroisocoumarin-type natural products, eurotiumide A and eurotiumide B have been described. The key features of these total syntheses are the asymmetric Shi epoxidation, regio- and stereoselective e

Synthesis, cytotoxicity and pro-apoptosis activity of isoquinoline quinones

Mansouramycins are newly isolated cytotoxic isoquinoline quinones from marine organism. To find novel anticancer agents, eighteen isoquinoline quinones 7a–7r as Mansouramycins analogs were designed and synthesized. Most of these compounds displayed modera

Total synthesis of the aglycone of IB-00208

Abstract A total synthesis of the aglycone of IB-00208 was accomplished in 22 steps using a newly developed approach towards polycyclic 1,4-dioxygenated xanthones from benzocyclobutenones. The generality of this entry to xanthones was initially established on several model systems before it was successfully applied to the construction of the hexacyclic core of the natural product. A new and potentially general approach towards angularly fused benzocyclobutenones using ring-closing metathesis (RCM) was also developed.