(5-Azido-2-formylphenoxy)acetic acid

Base Information

Chemical Name:(5-Azido-2-formylphenoxy)acetic acid
CAS No.:85819-05-2
Molecular Formula:C₉H₇N₃O₄
Molecular Weight:221.172
Hs Code.:
DSSTox Substance ID:DTXSID70561471
Wikidata:Q82445301

Synonyms:(5-azido-2-formylphenoxy)acetic acid;85819-05-2;DTXSID70561471

Suppliers and Price of (5-Azido-2-formylphenoxy)acetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of (5-Azido-2-formylphenoxy)acetic acid

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:221.04365571
Heavy Atom Count:16
Complexity:314

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C=C1N=[N+]=[N-])OCC(=O)O)C=O

Technology Process of (5-Azido-2-formylphenoxy)acetic acid

There total 1 articles about (5-Azido-2-formylphenoxy)acetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 144-48-9
iodacetamide

: 66761-28-2
4-azido-2-hydroxybenzaldehyde

: 85819-05-2
(5-azido-2-formylphenoxy)acetic acid

Guidance literature:: With sodium hydroxide; Multistep reaction; 1) EtOH, 2) DMF, 60 deg C, 1 h;
DOI:10.1021/jm00129a027

Reference yield:

: 85819-05-2
(5-azido-2-formylphenoxy)acetic acid

: 121329-86-0
9(S)-acetyl>amino>erythromycin

Guidance literature:: Multi-step reaction with 2 steps

1: 1) N-hydroxysuccinimide, N,N-dicyclohexylcarbodiimide / 1) 1,2-dimethoxyethane, room temperature, 3 h, than 0 deg C, overnight, 2) 0 deg C, overnight

2: NaBH₄ / ethanol / 3 h / 0 °C

With sodium tetrahydroborate; 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; In ethanol;
DOI:10.1021/jm00129a027

Reference yield:

erythromycylamine: 26116-56-3
erythromycylamine

: 85819-05-2
(5-azido-2-formylphenoxy)acetic acid

: 121329-85-9
9(S)-amino>erythromycin

Guidance literature:: With 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; Multistep reaction; 1) 1,2-dimethoxyethane, room temperature, 3 h, than 0 deg C, overnight, 2) 0 deg C, overnight;
DOI:10.1021/jm00129a027