2-Formylphenylboronic acid - CAS 40138-16-7
Catalog: |
BB024324 |
Product Name: |
2-Formylphenylboronic acid |
CAS: |
40138-16-7 |
Synonyms: |
(2-formylphenyl)boronic acid |
IUPAC Name: | (2-formylphenyl)boronic acid |
Description: | 2-Formylphenylboronic Acid can be used to prepare medicine for treating degenerative diseases of the elderly. |
Molecular Weight: | 149.94 |
Molecular Formula: | C7H7BO3 |
Canonical SMILES: | B(C1=CC=CC=C1C=O)(O)O |
InChI: | InChI=1S/C7H7BO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5,10-11H |
InChI Key: | DGUWACLYDSWXRZ-UHFFFAOYSA-N |
Boiling Point: | 355.7 °C at 760 mmHg |
Melting Point: | 115-120 °C (lit.) |
Flash Point: | Not applicable |
Purity: | 98 % |
Density: | 1.24 g/cm3 |
Appearance: | Light yellow to light orange-pink crystalline |
Storage: | 2-8 °C |
MDL: | MFCD00151822 |
LogP: | -0.82110 |
GHS Hazard Statement: | H315 (99.29%): 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-113321628-A | N-type organic dye based on benzothiazol and preparation method and application thereof | 20210528 |
CN-113150022-A | 3-substituted five-membered cyclic borate derivative, and pharmaceutical composition and pharmaceutical application thereof | 20210423 |
CN-113214302-A | 3-substituted five-membered cyclic borate derivative for inhibiting metal beta-lactamase and/or serine beta-lactamase | 20210423 |
CN-113155927-A | Glucose potential sensor based on SDBA-Au composite nanoenzyme | 20210401 |
CN-113024365-A | Industrial production method of benzo [ c ] phenanthrene-5-trifluoromethanesulfonate | 20210312 |
PMID | Publication Date | Title | Journal |
26734110 | 20150101 | Assembly of synthetic Aβ miniamyloids on polyol templates | Beilstein journal of organic chemistry |
22842531 | 20120914 | Schiff base formation and recognition of amino sugars, aminoglycosides and biological polyamines by 2-formyl phenylboronic acid in aqueous solution | Organic & biomolecular chemistry |
22735343 | 20120821 | Simple and efficient methods for discrimination of chiral diacids and chiral alpha-methyl amines | Organic & biomolecular chemistry |
22145800 | 20120106 | Three-component chiral derivatizing protocols for NMR spectroscopic enantiodiscrimination of hydroxy acids and primary amines | The Journal of organic chemistry |
21627154 | 20110805 | Asymmetric Strecker synthesis of α-arylglycines | The Journal of organic chemistry |
Complexity: | 138 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 150.0488242 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 150.0488242 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 57.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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