9-(4,6-dichloro-1,3,5-triazin-2-yl)-9H-carbazole

Name: 9-(4,6-dichloro-1,3,5-triazin-2-yl)-9H-carbazole
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CAS No. 24209-95-8
Cat. No. CS-0062096
Molecule weight315.16
Purity≥96%
MDL No.MFCD30562123

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9-(4,6-dichloro-1,3,5-triazin-2-yl)-9H-carbazole|CS-0062096

Structure of 24209-95-8

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General Information

CAS No. 24209-95-8
Cat. No. CS-0062096
Purity ≥96%
MDL No. MFCD30562123
Storage -20°C, sealed storage, away from moisture
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₅H₈Cl₂N₄
Molecular Weight 315.16
Synonym(s) 2,4-Dichlor-6-(9-carbazolyl)-1,3,5-triazin
SMILES N1(C=2C=CC=CC2C=3C=CC=CC31)C=4N=C(N=C(N4)Cl)Cl

Description

9-(4,6-Dichloro-1,3,5-triazin-2-yl)-9H-carbazole is a highly reactive triazine-based coupling reagent featuring two chlorine atoms at the 4- and 6-positions of the triazine ring. This configuration enables efficient activation of nucleophiles in amide bond formation and bioconjugation workflows. The electron-deficient triazine moiety readily engages with amines and hydroxyl groups under mild conditions. The carbazole scaffold provides enhanced stability and solubility in organic solvents. This compound serves as a robust linker in the synthesis of functionalized biomolecules and materials.

Application

9-(4,6-Dichloro-1,3,5-triazin-2-yl)-9H-carbazole serves as a versatile bifunctional building block for the synthesis of conjugated materials and functionalized heterocycles. The electrophilic triazine moiety enables efficient coupling with nucleophiles such as amines and alcohols under mild conditions, while the carbazole core provides robust stability and favorable electronic properties. Its bench-stable nature and clean reaction profile facilitate straightforward purification and scalability in synthetic workflows.

Safety Information

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GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

TPSA 43.6
LogP 4.2755
H_Acceptors 4
H_Donors 0
Rotatable_Bonds 1

Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Carbazole compounds

Building Blocks Skeleton Aromatic heterocycle compounds Triazine compounds

Key Words

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9-(4,6-dichloro-1,3,5-triazin-2-yl)-9H-carbazole

CAS No. 24209-95-8

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