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About This Item
線性公式:
C3H6O2BC6H3C(C8H17)2C6H3BO2C3H6
CAS號碼:
分子量：:
558.41
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.23
暫時無法取得訂價和供貨情況
推薦產品
品質等級
化驗
97%
mp
126-130 °C (lit.)
SMILES 字串
CCCCCCCCC1(CCCCCCCC)c2cc(ccc2-c3ccc(cc13)B4OCCCO4)B5OCCCO5
InChI
1S/C35H52B2O4/c1-3-5-7-9-11-13-21-35(22-14-12-10-8-6-4-2)33-27-29(36-38-23-15-24-39-36)17-19-31(33)32-20-18-30(28-34(32)35)37-40-25-16-26-41-37/h17-20,27-28H,3-16,21-26H2,1-2H3
InChI 密鑰
KAYXDWIILRESPY-UHFFFAOYSA-N
一般說明
It′s an aryl boronate ester. Arylboronic acids may be prepared by hydrolysis of boronate esters, and consequently many other boronic acid derivatives (e.g., organotrifluoroborates) are derived.[1]
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
An improved system for the palladium catalyzed borylation of aryl halides with pinacol borane
Billingsley KL, Buchwald SL
The Journal of Organic Chemistry, 73(14), 5589-5591 null
Paladium -catalyzed, direct boronic acide synthesis from aryl chlorides: A simplified route to diverse boronate ester derivatives
Molander GA,Trice SLJ, Dreher SD
Journal of the American Chemical Society, 132(50), 17701-17703 null
文章
Professor Chen (Nankai University, China) and his team explain the strategies behind their recent record-breaking organic solar cells, reaching a power conversion efficiency of 17.3%.
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