cas 175361-81-6|| where to buy 2,5-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene

Nom du produit:2,5-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene

IUPAC Name:4,4,5,5-tetramethyl-2-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl]-1,3,2-dioxaborolane

Unité d'emballage	Stock disponible	Prix($)
CM110000-5g	in stock	ȃľ
CM110000-10g	in stock	ŹŹ
CM110000-25g	in stock	Ǫŗƥ
CM110000-100g	in stock	ȃľŹ

Pour une utilisation en R&D uniquement..

Formulaire de demande

Nom chimique

Numéro CAS

Quantité*

Spécifications requises*
(% d'analyse, qualité du matériau, etc.)

Nom du contact*

Email du contact*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 175361-81-6 regularly via the above email.

Notes supplémentaires

Verification code*

refresh

: N° CAS:175361-81-6; Formule moléculaire:C16H26B2O4S; Point de fusion:-; Code SMILES:CC1(C)C(C)(C)OB(C2=CC=C(B3OC(C)(C)C(C)(C)O3)S2)O1; Densité:

: Numéro de catalogue:CM110000; Poids moléculaire:336.06; Point d'ébullition:434.3°C at 760 mmHg; N° Mdl:MFCD09800563; Stockage:

: Thiophenes; Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.

: Boronic Acids and Esters; Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).; Boronic Acid For Sale; Find trusted boronic acid for sale. Any requirements and problems can ask us at any time.

: Organic Photodiode (OPD); The most common type of organic photodetector is the organic photodiode (OPD). The photodiode has a simple structure in which an active layer is sandwiched between a transparent electrode and a metal electrode. In contrast to OLEDs, organic photodiodes (OPDs) utilize the organic semiconductor to absorb incident light and convert it to electric current. The structure and working principle are more like organic solar cells. Among the various organic photodetectors, organic photodiodes (OPDs) have been the most widely studied due to their fast response, high sensitivity, and full use of the existing research base of organic photovoltaics (OPVs).