2-Bromo-5-(tributylstannyl)pyridine

Product Information

Molecular Formula:
C17H30BrNSn
Molecular Weight:
447.04
Description
2-Bromo-5-(tributylstannyl)pyridine is a potent organostannane reagent. It is used in the biomedical industry for the synthesis of various bioactive compounds, particularly in anti-viral and anti-cancer drugs due to its biocompatible and efficient nature.
Synonyms
(6-bromopyridin-3-yl)-tributylstannane; 2-BROMO-5-(TRIBUTYLSTANNYL)PYRIDINE; 1008756-65-7; ACMC-20ao2a; SCHEMBL14120675; CTK6D4301
IUPAC Name
(6-bromopyridin-3-yl)-tributylstannane
Canonical SMILES
CCCC[Sn](CCCC)(CCCC)C1=CN=C(C=C1)Br
InChI
InChI=1S/C5H3BrN.3C4H9.Sn/c6-5-3-1-2-4-7-5;3*1-3-4-2;/h1,3-4H;3*1,3-4H2,2H3;
InChI Key
PHUCQXUSEZANQN-UHFFFAOYSA-N
Boiling Point
150-154 °C/2 mmHg
Flash Point
>230 °F
Purity
95%
Density
1.314 g/mL at 25 °C
Refractive Index
n20/D 1.537

Safety Information

Hazards
H301-H312-H315-H319-H372-H410
Precautionary Statement
P273-P280-P301 + P310-P305 + P351 + P338-P314-P501

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
10
Exact Mass
447.05837 g/mol
Monoisotopic Mass
447.05837 g/mol
Topological Polar Surface Area
12.9Ų
Heavy Atom Count
20
Formal Charge
0
Complexity
225
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
WO-2014022377-A1 Membranes and coatings made from mixtures including ionic liquids having silicon-bonded hydrolyzable groups 2012-07-30
CA-2837146-A1 Benzocycloheptene acetic acids 2011-06-06
EP-2718264-A1 Benzocycloheptene acetic acids 2011-06-06
EP-2718264-B1 Benzocycloheptene acetic acids 2011-06-06
JP-2014522407-A Benzocycloheptene acetic acid 2011-06-06
MX-2013013849-A ACIDS BENZOCICLOHEPTENO ACETICOS. 2011-06-06
US-2012309796-A1 Benzocycloheptene acetic acids 2011-06-06
WO-2012168162-A1 Benzocycloheptene acetic acids 2011-06-06
US-2003207910-A1 Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives 2001-02-02
US-2004110785-A1 Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives 2001-02-02
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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