製品名:6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4-tetrahydroisoquinoline

IUPAC Name:6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4-tetrahydroisoquinoline

CAS番号:922718-55-6
分子式:C15H22BNO2
純度:95%
カタログ番号:CM135218
分子量:259.16

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CM135218-10g in stock ȯǫȯǫ

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製品詳細

CAS番号:922718-55-6
分子式:C15H22BNO2
融点:-
SMILESコード:CC1(C)C(C)(C)OB(C2=CC3=C(CNCC3)C=C2)O1
密度:
カタログ番号:CM135218
分子量:259.16
沸点:
MDL番号:MFCD11044666
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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Tetrahydroisoquinolines
Tetrahydroisoquinoline is an organic compound with the chemical formula C9H11N. It is classified as a secondary amine, obtained from isoquinoline by hydrogenation. The tetrahydroisoquinoline moiety forms the backbone of several natural, synthetic and semi-synthetic drugs approved for the treatment of cancer, pain, gout and various neurodegenerative diseases.

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