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Merck

ALD00110

Sigma-Aldrich

Diethyl 1,2,3-triazine-4,6-dicarboxylate

≥95%

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100 MG
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100 MG
$247.00

About This Item

经验公式(希尔记法):
C9H11N3O4
分子量:
225.20
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

$247.00


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质量水平

方案

≥95%

表单

solid

储存温度

2-8°C

SMILES字符串

O=C(OCC)C1=NN=NC(C(OCC)=O)=C1

InChI

1S/C9H11N3O4/c1-3-15-8(13)6-5-7(11-12-10-6)9(14)16-4-2/h5H,3-4H2,1-2H3

InChI key

WSXMBZCJYIARRQ-UHFFFAOYSA-N

应用

1,2,3-Triazines have been shown to be reactive substrates in inverse electron demand Diels-Alder strategies. Recent examples by the Boger Research Group have utilized this reactive motif in the construction of highly functionalized N-containing heterocycles.

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


历史批次信息供参考:

分析证书(COA)

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Inverse electron demand Diels-Alder reactions enable total synthesis of natural products with heteroaromatic ring systems.

相关内容

The inverse electron demand Diels-Alder reactions of electron-deficient heterocycles are significant cycloaddition reactions for the total synthesis of natural products containing highly substituted and functionalized heteroaromatic ring systems.

Boger Lab utilizes nature's solutions in complex natural products, extending them through rational design for improved biological outcomes.

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