3337-66-4

Basic information

• Product Name: METHYL 3,5-DIIODO-4-HYDROXYBENZOATE
• Synonyms: METHYL 3,5-DIIODO-4-HYDROXYBENZOATE;RARECHEM AL BF 1485;4-Hydroxy-3,5-diiodo-benzoic acid Methyl ester;Methyl 4-hydroxy-3,5-diiodobenzoate
• CAS NO: 3337-66-4
• Molecular Formula: C₈H₆I₂O₃
• Molecular Weight: 403.94
• Mol File: 3337-66-4.mol
• Article Data: 17

Chemical Properties

• Melting Point: 167-168 °C
• Boiling Point: 328.257 °C at 760 mmHg
• Flash Point: 152.325 °C
• Appearance: /
• Density: 2.377 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.701
• Storage Temp.: 2-8°C(protect from light)
• PKA: 5.47±0.23(Predicted)
• CAS DataBase Reference: METHYL 3,5-DIIODO-4-HYDROXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3,5-DIIODO-4-HYDROXYBENZOATE(3337-66-4)
• EPA Substance Registry System: METHYL 3,5-DIIODO-4-HYDROXYBENZOATE(3337-66-4)

Safety Data

• Hazardous Substances Data: 3337-66-4(Hazardous Substances Data)

Usage

General Description

Methyl 3,5-diiodo-4-hydroxybenzoate is a chemical compound that belongs to the class of benzoic acid esters. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. METHYL 3,5-DIIODO-4-HYDROXYBENZOATE is known for its wide range of applications, including its use as an antifungal and antibacterial agent. It is also utilized in the production of various cosmetic and personal care products. Additionally, methyl 3,5-diiodo-4-hydroxybenzoate is an important reagent in organic synthesis and is widely used in research laboratories for various chemical reactions and experiments.

InChI:InChI=1/C8H6I2O3/c1-13-8(12)4-2-5(9)7(11)6(10)3-4/h2-3,11H,1H3

Upstream product

• 67-56-1 methanol 
• 618-76-8 3,5-diiodo-4-hydroxybenzoic acid 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 29289-13-2 2-iodo-4-methylaniline 
• 99-96-7 4-hydroxy-benzoic acid 
• 150-13-0 4-amino-benzoic acid 
• 190071-24-0 4-acetylamino-3-iodo-benzoic acid 
• 29289-16-5 N-(2-iodo-4-methylphenyl)acetamide 
• 2122-61-4 4-amino-3,5-diiodobenzoic acid 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 108839-23-2 3,5,3',5'-tetraiodo-4,4'-butanediyldioxy-di-benzoic acid dimethyl ester 
• 1245635-26-0 methyl 3,5-diiodo-4-(methoxymethoxy)benzoate 
• 19774-82-4 amiodarone hydrochloride 
• 1087223-70-8 C₂₆H₃₁I₂NO₄ 
• 1426673-14-4 4-formyl-2-iodo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl 2,4,5-trichlorobenzenesulfonate 
• 1426673-13-3 methyl 3-iodo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(((2,4,5-trichlorophenyl)sulfonyl)oxy)benzoate 
• 1426579-60-3 5-((4-chlorophenyl)(1H-1,2,4-triazol-1-yl)methyl)-1-methyl-1H-benzo[d]triazole 
• 120322-04-5 (4-chlorophenyl)(1-methyl-1H-1,2,3-benzotriazol-5-yl)methanol 
• 499770-67-1 1-methyl-1H-benzo[d][1,2,3]triazole-5-carbaldehyde 
• 1426579-79-4 4-(1,3-dioxolan-2-yl)-2-iodo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl 2,4,5-trichlorobenzenesulfonate 
• 1245635-30-6 methyl 3-iodo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethylsulfonyloxy)benzoate 
• 1245635-29-3 methyl 4-hydroxy-3-iodo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 

Relevant articles and documents

Design and construction of endo -functionalized multiferrocenyl hexagons via coordination-driven self-assembly and their electrochemistry

The construction of a new family of endo-functionalized multiferrocenyl hexagons with various sizes via coordination-driven self-assembly is described. The structures of these novel metallacycles, containing several ferrocenyl moieties at their interior s

Efficient and sustainable laccase-catalyzed iodination of: P -substituted phenols using KI as iodine source and aerial O2 as oxidant

The laccase-catalyzed iodination of p-hydroxyarylcarbonyl- and p-hydroxyarylcarboxylic acid derivatives using KI as iodine source and aerial oxygen as the oxidant delivers the corresponding iodophenols in a highly efficient and sustainable manner with yields up to 93% on a preparative scale under mild reaction conditions.

Method for synthesizing amiodarone impurity G and application of amiodarone impurity G

The invention provides a method for synthesizing an amiodarone impurity G and application of the amiodarone impurity G, and relates to the technical field of chemical synthesis. According to the method for synthesizing the amiodarone impurity G, the amiod