3-Pyridylboronic acid
Names
[ CAS No. ]:
1692-25-7
[ Name ]:
3-Pyridylboronic acid
[Synonym ]:
Acide pyridin-3-ylboronique
3-Pyridineboronic acid
Pyridin-3-bronic Acid
3-Pridylboronic acid
pyridin-3-yl boronic acid
3-Pyridylboronic aci
3-Pyridinylboronic acid
Boronic acid, B-3-pyridinyl-
pyridin-3-ylboronic acid
RARECHEM AH PB 0251
IFLAB-BB F1957-0039
3-pyridineboric acid
Pyridine-3-boronic Acid
3-Pyridylboronic acid
Pyridine-3-acid
MFCD00674177
3-PYRIDINEBORNIC ACID
3-pyridyl boronic acid
Biological Activity
[Description]:
[Related Catalog]:
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
308.8±34.0 °C at 760 mmHg
[ Melting Point ]:
>300 °C(lit.)
[ Molecular Formula ]:
C5H6BNO2
[ Molecular Weight ]:
122.92
[ Flash Point ]:
140.5±25.7 °C
[ Exact Mass ]:
123.049156
[ PSA ]:
53.35000
[ LogP ]:
0.10
[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C
[ Index of Refraction ]:
1.534
[ Storage condition ]:
0-6°C
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xn:Harmful
[ Risk Phrases ]:
R22;R36/37/38
[ Safety Phrases ]:
S36/37/39-S3-S26
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2933399090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2933399090
[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
Org. Biomol. Chem. 13th ed., 10 , 2683-2691, (2012)
An original tribromide derivative based, palladium-catalyzed synthesis of 3-substituted-1(2H)-isoquinolone is described based on a regioselective Suzuki-Miyaura C-C coupling on o-halo-(2,2-dihalovinyl...
Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors.Bioorg. Med. Chem. Lett. 5th ed., 22 , 1976-1979, (2012)
A series of P1-substituted biaryl amprenavir derivatives was designed and synthesized. These compounds were evaluated for enzyme inhibition and antiviral activity in vitro. Several compounds showed hi...
Copper-mediated sequential cyanation of aryl C-B and arene C-H bonds using ammonium iodide and DMF.J. Am. Chem. Soc. 5th ed., 134 , 2528-2531, (2012)
The cyanation of aromatic boronic acids, boronate esters, and borate salts was developed under copper-mediated oxidative conditions using ammonium iodide and DMF as the source of nitrogen and carbon a...