5-Aminopyrazine-2-carbaldehyde hydrochloride

Name: 5-Aminopyrazine-2-carbaldehyde hydrochloride
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CAS No. 1965308-99-9
Cat. No. CS-0102085
Purity≥95%
MDL No.None

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5-Aminopyrazine-2-carbaldehyde hydrochloride|CS-0102085

Structure of 1965308-99-9

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General Information

CAS No. 1965308-99-9
Cat. No. CS-0102085
Purity ≥95%
MDL No. None
Storage -20°C, sealed storage, away from moisture
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₅H₆ClN₃O
Molecular Weight 159.57
Synonym(s) 5-Amino-pyrazine-2-carbaldehyde hydrochloride
SMILES O=CC1=NC=C(N=C1)N.[H]Cl

Description

5-Aminopyrazine-2-carbaldehyde hydrochloride delivers a bifunctional scaffold combining an electron-rich amine and a reactive aldehyde group. This bench-stable derivative enables direct coupling in peptide conjugation and heterocycle synthesis, offering efficient access to bioactive nitrogen-containing architectures under standard conditions.

Application

5-Aminopyrazine-2-carbaldehyde hydrochloride serves as a versatile building block in medicinal chemistry, enabling direct incorporation of both amino and aldehyde functionalities into heterocyclic scaffolds. Its stability under standard reaction conditions facilitates downstream transformations such as reductive amination, condensation reactions, and transition metal-catalyzed couplings. The hydrochloride salt enhances solubility and handling, supporting efficient purification and scalability in API synthesis 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-P280-P302+P352

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Computational Chemistry Data

TPSA 68.87
LogP 0.2931
H_Acceptors 4
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Aldehyde

Building Blocks Skeleton Aromatic heterocycle compounds Pyrazine compounds

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5-Aminopyrazine-2-carbaldehyde hydrochloride

CAS No. 1965308-99-9

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