Azidoacetic acid methyl ester

Azidoacetic acid methyl ester
  • CAS No.:1816-92-8

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
Other grades of this product :
Azidoacetic acid methyl ester Basic information
Product Name:Azidoacetic acid methyl ester
Synonyms:Azidoacetic acid methyl ester;2-Azido-acetic acid Methyl ester;Acetic acid, 2-azido-, Methyl ester;Methyl 2-azidoacetate 97%;Methyl 2-azidoacetate - M3461
CAS:1816-92-8
MF:C3H5N3O2
MW:115.0907
EINECS:
Product Categories:
Mol File:1816-92-8.mol
Azidoacetic acid methyl ester Chemical Properties
Boiling point 35 °C
density 1.182 g/mL at 25 °C
refractive index n20/D1.440
Fp 48℃
Safety Information
Hazard Codes Xi
Risk Statements 5-10-36/37/38
Safety Statements 26
RIDADR UN 1993C 3 / PGIII
WGK Germany 3
MSDS Information
Azidoacetic acid methyl ester Usage And Synthesis
Uses
  • Methyl 2-azidoacetate is widely used as a precursor to build triazole derivatives via alkyne-azide click chemistry. Some of the examples include the synthesis of coumarin-triazole derivatives as potential antiplasmodial agents and macrocyclic triazole containing largazole analogs as histone deacetylases-1 (HDAC1) inhibitors.
  • It can be used to synthesize various pyrrole derivatives by Knoevenagel condensation as in the synthesis of near-infrared boron dipyrromethene (BODIPY) donors for organic tandem solar cells.
  • It can also be used in Hemetsberger-Knittel synthesis of substituted 5-, 6-, and 7-azaindoles.
  • Synthesis of highly fluorescent pyreno[2,1-b]pyrroles using methyl 2-azidoacetate as one of the reagents.

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