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ALD00110

Sigma-Aldrich

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

≥95%

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100 MG
$83.50

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100 MG
$83.50

About This Item

Empirical Formula (Hill Notation):
C9H11N3O4
Molecular Weight:
225.20
MDL number:
MFCD28411326
UNSPSC Code:
12352100
PubChem Substance ID:
329772593
NACRES:
NA.22

$83.50

List Price$167.00Save 50%
Web-Only Promotion

Available to ship onApril 25, 2025Details

Request a Bulk Order

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

Related Categories

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Articles

Inverse Electron Demand Diels-Alder Reactions

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

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Boger Group – Professor Product Portal

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

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