31252-85-4

Basic information

• Product Name: 4-NITROPHENYL IODOACETATE
• Synonyms: 4-NITROPHENYL IODOACETATE;LABOTEST-BB LT00847434;iodo-aceticaci4-nitrophenylester;P-NITROPHENYL IODOACETATE;4-NITROPHENYL IODOACETATE 99%;Iodoacetic acid 4-nitrophenyl ester;Iodo-acetic Acid p-Nitrophenyl Ester;4-Nitrophenyl 2-iodoacetate
• CAS NO: 31252-85-4
• Molecular Formula: C₈H₆INO₄
• Molecular Weight: 307.04
• EINECS: 250-536-6
• Product Categories: MTS and Sulfhydryl Active Reagents;MTS & Sulfhydryl Active Reagents;C8 to C9;Carbonyl Compounds;Esters;Building Blocks;C8 to C9;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
• Mol File: 31252-85-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: 79-82 °C
• Boiling Point: 383.8°C at 760 mmHg
• Flash Point: 185.9°C
• Appearance: /
• Density: 1.946g/cm³
• Vapor Pressure: 4.27E-06mmHg at 25°C
• Refractive Index: 1.643
• Storage Temp.: 2-8°C
• Solubility: Dichloromethane, Ether, Ethyl Acetate, Methanol
• BRN: 1970746
• CAS DataBase Reference: 4-NITROPHENYL IODOACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-NITROPHENYL IODOACETATE(31252-85-4)
• EPA Substance Registry System: 4-NITROPHENYL IODOACETATE(31252-85-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• RIDADR: 2811
• WGK Germany: 3
• F: 8-10
• HazardClass: 6.1(a)
• PackingGroup: II
• Hazardous Substances Data: 31252-85-4(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 31252-85-4 differently. You can refer to the following data:
1. A sulfhydryl reactive compound.
2. A sulfhydryl reactive compound

InChI:InChI=1/C8H6INO4/c9-5-8(11)14-7-3-1-6(2-4-7)10(12)13/h1-4H,5H2

Upstream product

• 100-02-7 4-nitro-phenol 
• 64-69-7 Iodoacetic acid 

Downstream Products

• 366446-41-5 p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate 
• 14609-74-6 p-nitrophenolate 
• 90764-56-0 (+)-S-2-amino-6-iodoacetamidohexanoic acid 
• 35748-65-3 (+)-S-2-amino-5-iodoacetamidopentanoic acid 

Relevant articles and documents

Synthesis of new photoaffine probes on the basis of ganglioside GM1

New photoaffine probes, photoreactive derivatives of ganglioside GM1 bearing a carbene-generating diazocyclopentadien-2-ylcarbonyl group at various distances from the carbohydrate moiety in their molecules were synthesized.

Regioselective synthesis of (+)-S-2-amino-5-iodoacetamidopentanoic and (+)-S-2-amino-6-iodoacetamidohexanoic acids

Mild reaction conditions were developed for the preparation of the active-site-directed irreversible enzyme inhibitors (+)-S-2-amino-5-iodoacetamido-pentanoic acid and (+)-S-2-amino-6-iodoacetamido-hexanoic acid.