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Merck
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文件

569356

Sigma-Aldrich

9,9-二辛基芴-2,7-二硼酸二(1,3-丙二醇)酯

97%

别名:

9,9-二辛基芴-2,7-二(硼酸三甲酯)

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About This Item

线性分子式:
C3H6O2BC6H3C(C8H17)2C6H3BO2C3H6
CAS号:
317802-08-7
分子量:
558.41
MDL號碼:
MFCD03701607
分類程式碼代碼:
12352103
PubChem物質ID:
24880496
NACRES:
NA.23

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

相关类别

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.

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)

分析证书(COA)

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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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