2-Formylphenylboronic acid - CAS 40138-16-7

Catalog:	BB024324
Product Name:	2-Formylphenylboronic acid
CAS:	40138-16-7
Synonyms:	(2-formylphenyl)boronic acid

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

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

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

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Related Functional Groups

Boronic Acids and Esters

[1022092-33-6]
1-(2-Cyanoethyl)-1H-pyrazole-4-boronic Acid Pinacol Ester
[1256355-43-7]
2-(Methoxycarbonyl)-4-methylphenylboronic Acid
[163105-90-6]
2-Methoxy-3-pyridylboronic Acid
[355836-10-1]
2-Methoxy-4-(trifluoromethoxy)phenylboronic Acid
[10365-98-7]
3-Methoxybenzeneboronic Acid
[470478-90-1]
4-(4-Boc-piperazino)phenylboronic Acid Pinacol Ester

Carbonyl Compounds

[91125-43-8]
Sulfophenyl nonanoate sodium salt
[51493-02-8]
N-Methyl-N-propylcarbamoyl Chloride
[1383427-98-2]
(S)-Hexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one hydrochloride
[35153-16-3]
(Z)-10-Tetradecenyl Acetate
[1006443-01-1]
1-(5-Nitropyridin-2-yl)-1H-pyrazole-3-carboxylic acid
[832741-29-4]
1-(4-Bromo-5-propylthiophen-2-yl)ethanone

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

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