89976-27-2

Basic information

• Product Name: METHYL 4-IODO-3-NITROBENZOATE
• Synonyms: METHYL 4-IODO-3-NITROBENZOATE;4-iodo-3-nitrobenzoic acid methyl ester;Methyl-4-iodo-3-nitrobenzoate SynonyMs 4-Iodo-3-Nitrobenzoic Acid Methyl Ester
• CAS NO: 89976-27-2
• Molecular Formula: C₈H₆INO₄
• Molecular Weight: 307.04
• Mol File: 89976-27-2.mol
• Article Data: 12

Chemical Properties

• Melting Point: 103-105°C
• Boiling Point: 360.1°C at 760 mmHg
• Flash Point: 171.6°C
• Appearance: /
• Density: 1.904g/cm³
• Vapor Pressure: 2.27E-05mmHg at 25°C
• Refractive Index: 1.631
• Storage Temp.: 2-8°C(protect from light)
• Water Solubility: Soluble in DCM 10mg/0.5mL. Insoluble in water.
• Sensitive: Light Sensitive
• CAS DataBase Reference: METHYL 4-IODO-3-NITROBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 4-IODO-3-NITROBENZOATE(89976-27-2)
• EPA Substance Registry System: METHYL 4-IODO-3-NITROBENZOATE(89976-27-2)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-37/39
• Hazardous Substances Data: 89976-27-2(Hazardous Substances Data)

Usage

Uses

Methyl 4-iodo-3-nitrobenzoate is used as pharmaceutical intermediate.

InChI:InChI=1/C8H6INO4/c1-14-8(11)5-2-3-6(9)7(4-5)10(12)13/h2-4H,1H3

Upstream product

• 619-44-3 methyl 4-iodobenzoate 
• 67-56-1 methanol 
• 35674-27-2 4-iodo-3-nitrobenzoic acid 
• 1588-83-6 4-amino-3-nitrobenzoic acid 
• 619-58-9 4-iodobenzoic acid 
• 1445-45-0 Trimethyl orthoacetate 
• 74-88-4 methyl iodide 

Downstream Products

• 98341-63-0 4-(5,6-dimethoxy-3-oxo-phthalan-4-yloxy)-3-nitro-benzoic acid methyl ester 
• 32117-05-8 methyl 3-nitro-4-(piperidin-1-yl)benzoate 
• 33358-30-4 3-nitro-4-phenylsulfanyl-benzoic acid methyl ester 
• 412947-54-7 methyl 3-amino-4-iodobenzoate 
• 39161-52-9 5[H]phenanthridin-6-one carboxylic acid 
• 51411-81-5 3-amino-4-iodo-benzoic acid 
• 1135859-04-9 C₂₀H₂₅N₃O₆ 
• 1321627-86-4 methyl 3-nitro-4-(phenylethynyl)benzoate 
• 1344728-39-7 C₁₃H₁₃NO₆ 

Relevant articles and documents

Modulating Guest Uptake in Core–Shell MOFs with Visible Light

A two-component core–shell UiO-68 type metal–organic framework (MOF) with a nonfunctionalized interior for efficient guest uptake and storage and a thin light-responsive outer shell was prepared by initial solvothermal MOF synthesis followed by solvent-as

HEPATITIS B CORE PROTEIN MODULATORS

The present disclosure provides, in part, compounds having allosteric effector properties against Hepatitis B virus Cp. Also provided herein are methods of treating viral infections, such as hepatitis B, comprising administering to a patient in need thereof a disclosed compound.

A significant enhancement of water vapour uptake at low pressure by amine-functionalization of UiO-67

The functionalization of UiO-67 with -NH2 groups enhances CO2 and CH4 adsorption at 1 bar and 298 K and positively influences the framework's interaction with water as evidenced by the significant enhancement of water vapo