5,5-Bis(tributylstannyl)-2,2-bithiophene

Product Information

Molecular Formula:
C32H58S2Sn2
Molecular Weight:
744.35
Description
5,5-Bis(tributylstannyl)-2,2-bithiophene is an indispensable compound applied in biomedicine to foster the emergence of potential therapeutic agents targeting an array of ailments. Distinguished by its distinctive architecture, it exhibits remarkable capabilities in combating cancer, diabetes, and neurodegenerative conditions.
Synonyms
Tributyl-[5-(5-tributylstannylthiophen-2-yl)thiophen-2-yl]stannane; 5,5'-Bis(tributylstannyl)-2,2'-bithiophene, 97%
IUPAC Name
tributyl-[5-(5-tributylstannylthiophen-2-yl)thiophen-2-yl]stannane
Canonical SMILES
CCCC[Sn](CCCC)(CCCC)C1=CC=C(S1)C2=CC=C(S2)[Sn](CCCC)(CCCC)CCCC
InChI
InChI=1S/C8H4S2.6C4H9.2Sn/c1-3-7(9-5-1)8-4-2-6-10-86*1-3-4-2/h1-4H6*1,3-4H2,2H3
InChI Key
HCHJCBXNKUSQOT-UHFFFAOYSA-N
Flash Point
230.0 °F - closed cup
Purity
97%
Density
1.217 g/mL at 25 °C

Safety Information

Hazards
H301 - H312 - H315 - H319 - H400
Precautionary Statement
P273 - P280 - P301 + P310 + P330 - P302 + P352 + P312 - P305 + P351 + P338

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
21
Exact Mass
744.20180 g/mol
Monoisotopic Mass
746.20240 g/mol
Topological Polar Surface Area
56.5Ų
Heavy Atom Count
36
Formal Charge
0
Complexity
463
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
CN-114181378-A Triaryl boron conjugated polymer porous material and preparation method and application thereof 2021-11-25
EP-3411374-A1 [1,5]naphthyridine compounds and polymers as semiconductors 2016-02-04
US-2019040188-A1 Organic semiconductors 2016-02-04
WO-2017133752-A1 [1,5]naphthyridine compounds and polymers as semiconductors 2016-02-04
US-10316060-B2 Energy transfer within pi-conjugated peptide heterostructures in aqueous environments 2014-11-24
US-2016145305-A1 Energy transfer within pi-conjugated peptide heterostructures in aqueous environments 2014-11-24
US-2014114052-A1 Palladium Catalyzed Reactions Executed on Solid-Phase Peptide Synthesis Supports for the Production of Self-Assembling Peptides Embedded with Complex Organic Electronic Subunits 2012-10-22
US-2015112044-A1 Palladium Catalyzed Reactions Executed on Solid-Phase Peptide Synthesis Supports for the Production of Self-Assembling Peptides Embedded with Complex Organic Electronic Subunits 2012-10-22
US-8871903-B2 Palladium catalyzed reactions executed on solid-phase peptide synthesis supports for the production of self-assembling peptides embedded with complex organic electronic subunits 2012-10-22
US-9234003-B2 Palladium catalyzed reactions executed on solid-phase peptide synthesis supports for the production of self-assembling peptides embedded with complex organic electronic subunits 2012-10-22
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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