794287
Bis[(pinacolato)boryl]methane
동의어(들):
2,2′-Methylenebis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane], Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methane
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모든 사진(2)
About This Item
실험식(Hill 표기법):
C13H26B2O4
CAS Number:
Molecular Weight:
267.97
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.22
추천 제품
양식
solid
Quality Level
환경친화적 대안 제품 특성
Catalysis
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48 °C
환경친화적 대안 카테고리
저장 온도
2-8°C
SMILES string
CC(C(C)(C)O1)(C)OB1CB2OC(C)(C)C(C)(C)O2
InChI
1S/C13H26B2O4/c1-10(2)11(3,4)17-14(16-10)9-15-18-12(5,6)13(7,8)19-15/h9H2,1-8H3
InChI key
MQYZGGWWHUGYDR-UHFFFAOYSA-N
일반 설명
Bis[(pinacolato)boryl]methane is an aryl boronate ester.
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애플리케이션
Bis-boronate has been reported by Morken and coworkers to be a key building block in the synthesis of enantioenriched secondary boronate esters, which undergo facile Suzuki-Miyaura coupling with minimal erosion of enantiopurity.
Bis[(pinacolato)boryl]methane may be used in the preparation of trans-vinyl boronate esters, via the Boron-Wittig reaction.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
이미 열람한 고객
A Catalytic Enantiotopic-Group-Selective Suzuki Reaction for the Construction of Chiral Organoboronates
Sun C, et al.
Journal of the American Chemical Society, 136, 6534-6537 (2014)
John R Coombs et al.
Organic letters, 17(7), 1708-1711 (2015-03-24)
A highly stereoselective boron-Wittig reaction between stable and readily accessible 1,1-bis(pinacolboronates) and aldehydes furnishes a variety of synthetically useful di- and trisubstituted vinyl boronate esters.
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