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ALD00104

Sigma-Aldrich

Methyl 1,2,3-triazine-4-carboxylate

Synonym(s):

1,2,3-Triazine-4-carboxylic acid, methyl ester

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About This Item

Empirical Formula (Hill Notation):
C5H5N3O2
CAS Number:
150017-41-7
Molecular Weight:
139.11
UNSPSC Code:
12352100
PubChem Substance ID:
329772590
NACRES:
NA.22

form

solid

storage temp.

2-8°C

SMILES string

O=C(OC)C1=CC=NN=N1

InChI

1S/C5H5N3O2/c1-10-5(9)4-2-3-6-8-7-4/h2-3H,1H3

InChI key

BYTPHJAFXFEZLP-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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Articles

Inverse Electron Demand Diels–Alder Reactions of 1,2,4,5-Tetrazines and 1,2,3-Triazines

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.

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