製品名:(4-[(TERT-BUTOXY)CARBONYL]-3-METHYLPHENYL)BORONIC ACID

IUPAC Name:{4-[(tert-butoxy)carbonyl]-3-methylphenyl}boronic acid

CAS番号:1246560-89-3
分子式:C12H17BO4
純度:95%+
カタログ番号:CM609405
分子量:236.07

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製品詳細

CAS番号:1246560-89-3
分子式:C12H17BO4
融点:-
SMILESコード:CC1=C(C=CC(=C1)B(O)O)C(=O)OC(C)(C)C
密度:
カタログ番号:CM609405
分子量:236.07
沸点:
MDL番号:MFCD18383511
保管方法:

Category 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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Column Infos

Encaleret
New England Journal of Medicine(NEJM) publication of positive encaleret proof-of-concept phase 2b results in patients with autosomal dominant hypocalcemia type 1 (ADH1).
Encaleret is an investigational, orally administered small molecule that selectively antagonizes the calcium sensing receptor (CaSR), targeting ADH1 at its source. If approved, encaleret could be the first therapy specifically indicated for the treatment of ADH1.
Encaleret has received fast track designation by the U.S. FDA and orphan drug designation in the United States and the European Union.

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