Nom du produit:dimethyl({[3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl})amine

IUPAC Name:dimethyl({[3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl})amine

CAS:2369772-15-4
Formule moléculaire:C16H26BNO2
Pureté:95%+
Numéro de catalogue:CM1077583
Poids moléculaire:275.2

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CM1077583-1g in stock ʼnNJưƞ

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Détails du produit

N° CAS:2369772-15-4
Formule moléculaire:C16H26BNO2
Point de fusion:-
Code SMILES:CN(C)CC1=CC=C(B2OC(C)(C)C(C)(C)O2)C(C)=C1
Densité:
Numéro de catalogue:CM1077583
Poids moléculaire:275.2
Point d'ébullition:
N° Mdl:
Stockage:

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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ORIC-944
ORIC-944 is a potent and selective allosteric inhibitor of PRC2 developed by ORIC Pharmaceuticals. Initiated dosing of ORIC-944 in combination with NUBEQA® (darolutamide) and in combination with ERLEADA® (apalutamide) in the ongoing Phase 1b trial for prostate cancer in first half of 2024. Entered into clinical trial collaboration and supply agreements with Bayer and Johnson & Johnson to support the ongoing Phase 1b trial of ORIC-944 in combinations with AR inhibitors for the treatment of prostate cancer.
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