131088-03-4

Basic information

• Product Name: 2,4-dihydroxy-5-iodobenzaldehyde
• Synonyms: 2,4-dihydroxy-5-iodobenzaldehyde;Benzaldehyde, 2,4-dihydroxy-5-iodo-
• CAS NO: 131088-03-4
• Molecular Formula: C₇H₅IO₃
• Molecular Weight: 264.01727
• Mol File: 131088-03-4.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4-dihydroxy-5-iodobenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dihydroxy-5-iodobenzaldehyde(131088-03-4)
• EPA Substance Registry System: 2,4-dihydroxy-5-iodobenzaldehyde(131088-03-4)

Safety Data

• Hazardous Substances Data: 131088-03-4(Hazardous Substances Data)

Usage

General Description

2,4-dihydroxy-5-iodobenzaldehyde is a chemical compound with molecular formula C7H5IO3. It is a yellow crystalline solid that is used in the synthesis of various organic compounds. 2,4-dihydroxy-5-iodobenzaldehyde contains two hydroxyl groups and one iodine atom attached to a benzene ring with an aldehyde functional group. It has been reported to exhibit moderate antibacterial and antifungal activities. It is also used as a reagent in organic synthesis and as a starting material in the production of various pharmaceuticals and agrochemicals.

Upstream product

• 95-01-2 2,4-Dihydroxybenzaldehyde 

Downstream Products

• 1400807-67-1 2,4-bis(allyloxy)-5-iodobenzaldehyde 
• 1252581-54-6 6-hydroxy-2-(3,5-dihydroxyphenyl)benzofuran-5-carbaldehyde 

Relevant articles and documents

MOLECULES PRESENTING DUAL EMISSION PROPERTIES

The present invention concerns compound of formula (I): wherein: - A represents an electron-withdrawing group; - D represents an electron-donating group; - X is selected from the group consisting of: O, S and NR, wherein R is selected from the group consi

Facile synthesis of natural moracin compounds using PD(OAC)2/P(TBU)3-HBF4 as a sonogashira coupling reagent

An efficient and practical synthesis of natural moracins, which have diverse range of biological properties including anticancer, antioxidant, and antibacterial activities, has been achieved using Pd(OAc)2/P(tBu)3-HBF

The first total synthesis of moracin O and moracin P, and establishment of the absolute configuration of moracin O

The first total synthesis of the naturally occurring benzofurans, moracins O and P was achieved using a Sonogashira cross coupling reaction followed by in situ cyclization, and the absolute configuration of natural moracin O was established.