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636010

3,5-二甲基吡唑-4-硼酸频那醇酯

Name: 3,5-二甲基吡唑-4-硼酸频那醇酯
Brand: ALDRICH

97%

别名:

3,5-二甲基-4-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)-1H-吡唑, 3,5-二甲基-4-吡唑硼酸频哪醇酯

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关于此项目

经验公式（希尔记法）:

C₁₁H₁₉BN₂O₂

化学文摘社编号:

857530-80-4

分子量:

222.09

NACRES:

NA.22

PubChem Substance ID:

24882751

UNSPSC Code:

12352103

MDL number:

MFCD05663852

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属性

Quality Level

100

assay

97%

form

solid

mp

163-168 °C (lit.)

SMILES string

Cc1n[nH]c(C)c1B2OC(C)(C)C(C)(C)O2

InChI

1S/C11H19BN2O2/c1-7-9(8(2)14-13-7)12-15-10(3,4)11(5,6)16-12/h1-6H3,(H,13,14)

InChI key

GNUDAJTUCJEBEI-UHFFFAOYSA-N

说明

Application

3,5-Dimethylpyrazole-4-boronic acid pinacol ester can be used:

To synthesize 9H-pyrimido[4,5-b]indole and aryl-benzimidazole based BET bromodomain and extra terminal (BET) protein inhibitors.
To prepare naphthalimide based photo-exchangeable photochromic fluorescent molecules.
As a reactant to develop DNA-encoded chemical libraries by palladium-catalyzed Suzuki coupling reaction with DNA-linked aryl halides.

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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商品

Suzuki-Miyaura Cross-Coupling Reagents

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

Structure-guided discovery of a novel, potent, and orally bioavailable 3, 5-dimethylisoxazole aryl-benzimidazole BET bromodomain inhibitor

Sperandio D, et al.

Bioorganic & Medicinal Chemistry, 27(3), 457-469 (2019)

Development of DNA-compatible suzuki-miyaura reaction in aqueous media

Li J and Huang H

Bioconjugate Chemistry, 29(11), 3841-3846 (2018)

Investigation of Photochromic Fluorescence Features and Synthesis of Diarylethene Type Naphthalimide Compounds

Orhan E and Narin M

Journal of the Turkish Chemical Society Section A: Chemistry, 7(1), 97-106 (2020)

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全球贸易项目编号

货号	GTIN
636010-5G	04061832880433
636010-1G	04061826065440