cas 1339890-99-1|| where to buy 1-(oxetan-3-yl)-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

Product Name:1-(oxetan-3-yl)-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

IUPAC Name:1-(oxetan-3-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

: CAS：1339890-99-1; Molecular Formula：C12H19BN2O3; Purity：95%+

: Catalog Number：CM106517; Molecular Weight：250.11

Packing Unit	Available Stock	Price($)
CM106517-250mg	in stock	Ȏź
CM106517-1g	in stock	ŉǵŉ
CM106517-5g	in stock	Ţǵư
CM106517-10g	in stock	ǵĽǊŉ

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Product Details

: CAS NO:1339890-99-1; Molecular Formula:C12H19BN2O3; Melting Point:-; Smiles Code:CC1(C)OB(C2=CN(C3COC3)N=C2)OC1(C)C; Density:

: Catalog Number:CM106517; Molecular Weight:250.11; Boiling Point:384.7±32.0°C; MDL No:; Storage:2-8°C

Category Infos

: Pyrazoles; Pyrazoles are organic compounds of the general formula C3H3N2H. It is a five-membered heterocycle consisting of three carbon atoms and two adjacent nitrogen atoms. As an H-bond-donating heterocycle, pyrazole has been used as a more lipophilic and metabolically more stable bioisomer of phenol. Pyrazoles have attracted more and more attention due to their broad spectrum of action and strong efficacy.; Pyrazone; Custom pyrazone for customers from all over the world are our main business.

: Oxetanes; Oxygen heterocycles are one of the most common heterocycles in drugs and natural products. Oxetene has high polarity and is also a good acceptor for hydrogen bond, which contributes to the metabolism and chemical stability of its host molecules. When substituted for commonly used functional groups such as gem dimethyl or carbonyl, oxetane units can induce profound changes in water solubility, lipophilicity, metabolic stability and conformational preference. Four of the FDA-approved drugs contain oxetenes: Orlistat, Paclitaxel, and two of its derivatives, Docetaxel and Cabazitaxel. Currently, oxetane-containing building blocks are flourishing in medicinal chemistry and drug discovery.

Column Infos

: 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).

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