Merck

632732

Sigma-Aldrich

1-Boc-吡唑-4-硼酸频哪醇酯

97%

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别名:
1-叔丁氧羰基-吡唑-4-硼酸频哪醇酯, 4-(4,4,5,5-四甲基-1,3,2-二氧杂环硼戊烷-2-基)-1-Boc-吡唑, 4-(4,4,5,5-四甲基-1,3,2-二氧杂环硼戊烷-2-基)-1-吡唑羧酸叔丁酯
Empirical Formula (Hill Notation):
C14H23BN2O4
分子量:
294.15
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

形式

solid

mp

82-86 °C (lit.)

储存温度

2-8°C

SMILES string

CC(C)(C)OC(=O)n1cc(cn1)B2OC(C)(C)C(C)(C)O2

InChI

1S/C14H23BN2O4/c1-12(2,3)19-11(18)17-9-10(8-16-17)15-20-13(4,5)14(6,7)21-15/h8-9H,1-7H3

InChI key

IPISOFJLWYBCAV-UHFFFAOYSA-N

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此商品
721344525057595314
4-Pyrazoleboronic acid pinacol ester 97%

Sigma-Aldrich

525057

4-吡唑硼酸频哪醇酯

form

solid

form

solid

form

solid

form

solid

mp

82-86 °C (lit.)

mp

72-76 °C

mp

142-146 °C (lit.)

mp

59-64 °C (lit.)

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

-

storage temp.

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

应用

Reagent used for
  • Suzuki Coupling
  • Copper-catalyzed azidation

Reagent used in Preparation of
  • Selective quinazolinyl-phenol inhibitors of CHK1 as potential antitumors and radioprotectants
  • Stereoselective synthesis of selective Cathepsin inhibitors

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

Eyeshields, Gloves, type N95 (US)


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其他客户在看

Slide 1 of 3

1 of 3

John J Caldwell et al.
Journal of medicinal chemistry, 54(2), 580-590 (2010-12-29)
Structure-based design was applied to the optimization of a series of 2-(quinazolin-2-yl)phenols to generate potent and selective ATP-competitive inhibitors of the DNA damage response signaling enzyme checkpoint kinase 2 (CHK2). Structure-activity relationships for multiple substituent positions were optimized separately and
Copper(II)-catalyzed conversion of aryl/heteroaryl boronic acids, boronates, and trifluoroborates into the corresponding azides: substrate scope and limitations
K. D. Grimes, et al.,
Synthesis, 9, 1441-1448 (2010)
Paul A Bethel et al.
Bioorganic & medicinal chemistry letters, 19(16), 4622-4625 (2009-07-21)
A number of molecular recognition features have been exploited in structure-based design of selective Cathepsin inhibitors.

商品

The Suzuki-Miyaura cross-coupling reaction is an important and extensively used reaction in organic chemistry with applications in polymer science and in the fine chemicals and pharmaceutical industries.

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