2-chloro-5-(tributylstannyl)pyrimidine

Product Information

Molecular Formula:
C16H29ClN2Sn
Molecular Weight:
403.58
Description
2-Chloro-5-(tributylstannyl)pyrimidine is a chemical compound mainly used in medicinal chemistry research. It participates as a reagent in the synthesis of stannylated pyrimidine derivatives, which can further be used for development of antiviral and anticancer drugs.
Synonyms
Tributyl-(2-chloropyrimidin-5-yl)stannane; 2-Chloro-5-(tri-n-butylstannyl)pyrimidine; 2-Chloro-5-(tributylstannyl)pyrimidine, 95%; 2-Chloro-5-(tri-N-butylstannyl)pyrimidine,95%
IUPAC Name
tributyl-(2-chloropyrimidin-5-yl)stannane
Canonical SMILES
CCCC[Sn](CCCC)(CCCC)C1=CN=C(N=C1)Cl
InChI
InChI=1S/C4H2ClN2.3C4H9.Sn/c5-4-6-2-1-3-7-43*1-3-4-2/h2-3H3*1,3-4H2,2H3
InChI Key
JEHJKYNDOIGAEA-LLWNALMOAU
Flash Point
Not applicable
Purity
95%
Density
1.222 g/mL at 25 °C
Refractive Index
n20/D 1.522

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
2
Rotatable Bond Count
10
Exact Mass
404.104129 g/mol
Monoisotopic Mass
404.104129 g/mol
Topological Polar Surface Area
25.8Ų
Heavy Atom Count
20
Formal Charge
0
Complexity
221
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
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
US-2005090522-A1 Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives 2001-02-02
US-2008119480-A1 Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives 2001-02-02
US-2009306095-A1 Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives 2001-02-02
US-2010093752-A1 Pharmaceutical formulations of substituted azaindoleoxoacetic piperazine derivatives with protease inhibitors 2001-02-02
US-2011118279-A1 Pharmaceutical formulations of substituted azaindoleoxoacetic piperazine derivatives with protease inhibitors 2001-02-02
US-2011245268-A1 Pharmaceutical formulations of substituted azaindoleoxoacetic piperazine derivatives with protease inhibitors 2001-02-02
US-2012095017-A1 Pharmaceutical formulations of substituted azaindoleoxoacetic piperazine derivatives with protease inhibitors 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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