3-Aminobenzeneboronic Acid - CAS 30418-59-8
Catalog: |
BB020588 |
Product Name: |
3-Aminobenzeneboronic Acid |
CAS: |
30418-59-8 |
Synonyms: |
(3-aminophenyl)boronic acid; (3-aminophenyl)boronic acid |
IUPAC Name: | (3-aminophenyl)boronic acid |
Description: | 3-Aminophenylboronic acid (3-APBA) can undergo three-component condensation with 3,5-disubstituted salicylaldehyde derivatives and aliphatic alcohols to afford calix-shaped boron complexes. Due to its ability to selectively bind with diol-compounds, 3-APBA can be employed in developing sensors for detecting saccharides and glycosylated biomolecules by immobilizing on a metal substrate via a self-assembled monolayer. This product was previously listed as CDS003827. |
Molecular Weight: | 136.94 |
Molecular Formula: | C6H8NO2B |
Canonical SMILES: | B(C1=CC(=CC=C1)N)(O)O |
InChI: | InChI=1S/C6H8BNO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4,9-10H,8H2 |
InChI Key: | JMZFEHDNIAQMNB-UHFFFAOYSA-N |
Boiling Point: | 376 °C at 760 mmHg |
Melting Point: | 225 °C |
Flash Point: | Not applicable |
Density: | 1.23 g/cm3 |
MDL: | MFCD00007755 |
LogP: | -0.47020 |
GHS Hazard Statement: | H315 (97.78%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113499435-A | Up-conversion fluorescent artificial antibody, preparation method and application thereof | 20210628 |
CN-113416235-A | Liquid chromatography for purifying and separating virus antigens | 20210624 |
CN-113304708-A | Preparation method of glycoprotein microreactor with boron affinity surface imprinting of mesoporous molecular sieve | 20210611 |
CN-113354810-A | Clustering peptide with side chain containing functionalized biphenyl group and preparation method thereof | 20210607 |
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PMID | Publication Date | Title | Journal |
23010222 | 20121115 | Mechanisms for epigallocatechin gallate induced inhibition of drug metabolizing enzymes in rat liver microsomes | Toxicology letters |
22820862 | 20121004 | Cell surface carbohydrates evaluation via a photoelectrochemical approach | Chemical communications (Cambridge, England) |
22840004 | 20121001 | Synthesis and characterization of a novel boronic acid-functionalized chitosan polymeric nanosphere for highly specific enrichment of glycopeptides | Carbohydrate polymers |
22947052 | 20120919 | Self-propelled carbohydrate-sensitive microtransporters with built-in boronic acid recognition for isolating sugars and cells | Journal of the American Chemical Society |
22341749 | 20120801 | [Clinical and epidemiological study of an outbreak of KPC-producing Klebsiella pneumoniae infection in Buenos Aires, Argentina] | Enfermedades infecciosas y microbiologia clinica |
Complexity: | 110 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 137.0648087 |
Formal Charge: | 0 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 3 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 137.0648087 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 66.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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