跳转至内容
Merck
CN

主要文件

查看所有文档

ALD00110

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

≥95%

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式（希尔记法）:
C9H11N3O4
分子量:
225.20
MDL number:
MFCD28411326
UNSPSC Code:
12352100
PubChem Substance ID:
329772593
NACRES:
NA.22
Assay:
≥95%
Form:
solid
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

Quality Level

100

assay

≥95%

form

solid

storage temp.

2-8°C

SMILES string

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

Application

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.

Other Notes

Inverse Electron Demand Diels–Alder Reactions of 1, 2, 3-Triazines: Pronounced Substituent Effects on Reactivity and Cycloaddition Scope
Total Syntheses of (-)-Pyrimidoblamic Acid and P-3A

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

新产品

此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助，请联系 客户支持

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

商品

Inverse Electron Demand Diels-Alder Reactions

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

相关内容

Boger Group – Professor Product Portal

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

全球贸易项目编号

货号GTIN
ALD00110-100MG04061833244678