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线性分子式:
C3H6O2BC6H3C(C8H17)2C6H3BO2C3H6
化学文摘社编号:
分子量:
558.41
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
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
SMILES string
CCCCCCCCC1(CCCCCCCC)c2cc(ccc2-c3ccc(cc13)B4OCCCO4)B5OCCCO5
InChI key
KAYXDWIILRESPY-UHFFFAOYSA-N
assay
97%
mp
126-130 °C (lit.)
Quality Level
General description
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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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
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