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
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 |
