4-(Tributylstannyl)thiazole

Product Details

CAS No:173979-01-6

MF:C15H29NSSn

Appearance:colorless or light-yellow transparent liquid

Specification:98.5%

UN number:UN 2788 6.1/PG III

Package:1/5/10/25kgs/drum

Supply Capacity:KGS

Synonyms:4-(TRIBUTYLSTANNYL)THIAZOLE;(1,3-Thiazol-4-yl)tributylstannane;(Thiazol-4-yl)tributylstannane;4-(Tributylstannanyl)-1,3-thiazole;4-(Tributylstannyl);Thiazole,4-(tributylstannyl)-;TRIBUTYL(1,3-THIAZOL-4-YL)STANNANE;4-(Tri-n-butylstannyl)thiazole, 95%; 4-(tri-n-butylstannyl)thiazole; RefChem:517053; 677-930-4; 4-(Tributylstannyl)thiazole; 173979-01-6; 4-(Tributylstannyl)-1,3-thiazole; Thiazole, 4-(tributylstannyl)-; tributyl(1,3-thiazol-4-yl)stannane; tributyl(thiazol-4-yl)stannane; MFCD01319073; 4-tributylstannylthiazole; 4-(tributylstannanyl)-1,3-thiazole; 4-tributylstannyl thiazole; 4-tributylstannanyl-thiazole; 4-tri-n-butylstannylthiazole; SCHEMBL41732; 4-tributylstannyl-1,3-thiazol; tributyl(1,3-thiazol4-yl)tin; tributyl(1,3-thiazol-4-yl)tin; DTXSID50376848; YYQKQPYPLADFMK-UHFFFAOYSA-N; 4-tri-n-butylstannyl-1,3-thiazole; YGA97901; AKOS015843335; GS-6492; 4-(tributylstannyl)thiazole, AldrichCPR; SY033614; DB-106204; CS-0040966; EN300-184306; F11321

Product application:4-(Tributylstannyl)thiazole,173979-01-6,4-Tributylstannylthiazole,4-(tri-n-butylstannyl)thiazole,4-(tributylstannyl)-1,3-thiazole,Thiazol-4-yltributylstannane,Stille coupling reagent,Organotin reagent,Palladium-catalyzed cross-coupling synthon,Thiazole heterocyclic building block,Pharmaceutical grade 4-(Tributylstannyl)thiazole,Targeted oncology API intermediate,Antiviral drug precursor,Kinase inhibitor building block,OLED optoelectronic intermediate,Organic semiconductor monomer,Conjugated polymer building block,Fine chemical intermediate,High purity 4-(Tributylstannyl)thiazole 98%,4-(Tributylstannyl)thiazole manufacturer China,CAS 173979-01-6 supplier,Suzhou Health Chemicals organotin reagents,4-Tributylstannylthiazole wholesale bulk export

 

4-(Tributylstannyl)thiazole serves as an indispensable, high-purity heteroaromatic organotin building block, premier Stille cross-coupling nucleophilic reagent, and versatile heterocyclic synthon extensively utilized across targeted biopharmaceuticals, active pharmaceutical ingredient (API) manufacturing, advanced organic optoelectronics, semiconducting conjugated polymers, and fine organic synthesis sectors. In commercial pharmaceutical manufacturing and medicinal chemistry discovery, universally recognized as Thiazol-4-yltributylstannane, its distinctive structural hallmark resides in the precise placement of a tri-n-butylstannyl handle at the C4 position of the electron-deficient 1,3-thiazole nucleus; this architecture enables exceptionally smooth, regioselective palladium-catalyzed Stille cross-coupling transformations with a broad range of aryl halides, heteroaryl bromides, iodides, and pseudo-halides under mild, neutral, and highly functional-group-compatible conditions without disturbing fragile esters, amides, or carbamates, functioning as an irreplaceable tool for installing 4-substituted thiazole pharmacophores to assemble targeted protein kinase inhibitors, antineoplastic clinical candidates, broad-spectrum antiviral agents, and neuroprotective therapeutic platforms. In organic semiconductor electronics and photonic display engineering, because the planar thiazole heterocycle imparts favorable pi-pi stacking, tunable frontier molecular orbital energy levels, and balanced dipolar properties, this organometallic building block is universally deployed to construct narrow-bandgap push-pull alternating conjugated polymers, organic field-effect transistor (OFET) transport layers, and high-efficiency electron-transport and host materials for modern OLED devices. In macromolecular science and smart responsive polymers, it is incorporated into rigid-rod conjugated polymer backbones to fabricate electrochromic films, specialty photoluminescent sensing probes, and thermo-stable organic conductors. In functional adhesives, specialty aerospace coatings, and electronic packaging matrices, its heterocyclic chelating derivatives enhance micro-scale interfacial anchoring and moisture-resistant mechanical adhesion onto precious metal and copper substrates. Furthermore, in the discovery of novel heterocyclic agricultural crop fungicides, bio-imaging molecular sensors, and coordination corrosion inhibition agents for petroleum and natural gas exploration pipelines, chemical architectures engineered from 4-(Tributylstannyl)thiazole deliver outstanding chemical reactivity, structural versatility, and broad multi-industry performance.