3-Pyridylboronic acid
Suppliers
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
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...
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...
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...