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Merck
CN

574686

Sigma-Aldrich

3-氨基苯硼酸频哪醇酯

97%

别名:

3-(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)苯胺

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About This Item

经验公式(希尔记法):
C12H18BNO2
分子量:
219.09
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

mp

90-94 °C (lit.)

SMILES字符串

CC1(C)OB(OC1(C)C)c2cccc(N)c2

InChI

1S/C12H18BNO2/c1-11(2)12(3,4)16-13(15-11)9-6-5-7-10(14)8-9/h5-8H,14H2,1-4H3

InChI key

YMXIIVIQLHYKOT-UHFFFAOYSA-N

应用

3-Aminophenylboronic acid pinacol ester can be used:
  • As a starting material for the synthesis of 6-(hetero)arylthieno[3,2-b]pyridines, which are known to inhibit human tumor cells selectively.
  • In the functionalization of deuteroporphyrin IX dimethyl ester through Suzuki-Miyaura coupling.
  • To prepare benzo[d]oxazole based type-I FLT3-ITD inhibitors.

法律信息

Boron Molecular 产品

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Functionalization of Deutero-and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions
O?Brien JM, et al.
The Journal of Organic Chemistry, 84(10), 6158-6173 (2019)
Discovery of benzo [d] oxazole derivatives as the potent type-I FLT3-ITD inhibitors
Bao J, et al.
Bioorganic Chemistry, 94(10), 103248-103248 (2020)
Efficient synthesis of 6-(hetero) arylthieno [3, 2-b] pyridines by Suzuki-Miyaura coupling. Evaluation of growth inhibition on human tumor cell lines, SARs and effects on the cell cycle
Queiroz M-J, et al.
European Journal of Medicinal Chemistry, 45(12), 5628-5634 (2010)

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