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632732

Sigma-Aldrich

1-Boc-吡唑-4-硼酸频哪醇酯

97%

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

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About This Item

经验公式（希尔记法）:
C14H23BN2O4
分子量:
294.15
MDL號碼:
MFCD05663873
分類程式碼代碼:
12352103
PubChem物質ID:
24882509
NACRES:
NA.22

品質等級

100

化驗

97%

形狀

solid

mp

82-86 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

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 密鑰

IPISOFJLWYBCAV-UHFFFAOYSA-N

相关类别

應用

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

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)

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分析证书(COA)

Lot/Batch Number
MKCK0294
MKBJ7503V
MKBG5798V
MKBD9142V
73596PJ

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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)
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
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

Suzuki–Miyaura Coupling Reagents

This brochure contains a comprehensive selection of boronic acids, boronic acid esters, diboron esters, and transition-metal catalysts useful for the Suzuki–Miyaura coupling reaction

Suzuki–Miyaura Coupling Reagents

This brochure contains a comprehensive selection of boronic acids, boronic acid esters, diboron esters, and transition-metal catalysts useful for the Suzuki–Miyaura coupling reaction

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