2-Acrylamidophenylboronic acid

Base Information

• Chemical Name: 2-Acrylamidophenylboronic acid
• CAS No.: 758697-66-4
• Molecular Formula: C₉H₁₀BNO₃
• Molecular Weight: 190.994
• Hs Code.: 2931900090
• DSSTox Substance ID: DTXSID10597239
• Nikkaji Number: J1.559.946D
• Mol file: 758697-66-4.mol

Synonyms:2-Acrylamidophenylboronic acid;758697-66-4;(2-Acrylamidophenyl)boronic acid;[2-(prop-2-enoylamino)phenyl]boronic acid;2-Acrylamido-phenylboronic acid;[2-(prop-2-enamido)phenyl]boronic acid;SCHEMBL236887;(2-Acrylamidophenyl)boronicacid;DTXSID10597239;XGDUBFMBDDZYKB-UHFFFAOYSA-N;MFCD12756424;[2-(Acryloylamino)phenyl]boronic acid;AKOS006346586;BS-22837;DB-364546;CS-0173991;2-(PROP-2-ENAMIDO)PHENYLBORONIC ACID;A865603

Chemical Property of 2-Acrylamidophenylboronic acid

Chemical Property:

• PKA: 8.48±0.53(Predicted)
• Density: 1.22±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 191.0753733
• Heavy Atom Count: 14
• Complexity: 220

Purity/Quality:

97% ^*data from raw suppliers

2-AcrylamidophenylboronicAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: B(C1=CC=CC=C1NC(=O)C=C)(O)O
• Uses: 2-Acrylamidophenylboronic acid has been study for the potential to be used as a glucose-?selective holographic sensors due to 2-Acrylamidophenylboronic acid ability to bind to glucose.

Technology Process of 2-Acrylamidophenylboronic acid

There total 1 articles about 2-Acrylamidophenylboronic 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: 50.0%

2-amino-benzeneboronic acid hydrochloride + acryloyl chloride (814-68-6,25189-84-8) → 2-acrylamidophenylboronic acid (758697-66-4)

Guidance literature:

In sodium hydroxide; at 20 ℃; for 2h;

DOI:10.1002/chem.200600442

upstream raw materials:

acryloyl chloride