49541-79-9

Basic information

• Product Name: 2-Hydrazino-1,4,5,6-tetrahydropyrimidine hydroiodide
• Synonyms: 2-Hydrazino-1,4,5,6-tetrahydropyrimidine hydroiodide;1,4,5,6-TETRAHYDROPYRIMIDIN-2-HYDRAZINE HYDROBROMIDE
• CAS NO: 49541-79-9
• Molecular Formula: C₄H₁₀N₄*HI
• Molecular Weight: 242.06141
• Product Categories: Ring Systems
• Mol File: 49541-79-9.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Hydrazino-1,4,5,6-tetrahydropyrimidine hydroiodide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Hydrazino-1,4,5,6-tetrahydropyrimidine hydroiodide(49541-79-9)
• EPA Substance Registry System: 2-Hydrazino-1,4,5,6-tetrahydropyrimidine hydroiodide(49541-79-9)

Safety Data

• Hazardous Substances Data: 49541-79-9(Hazardous Substances Data)

Upstream product

• 5445-73-8 2-methylthio-1,4,5,6-tetrahydropyrimidine hydroiodide 
• 2055-46-1 3,4,5,6-tetrahydropyrimidine-2-thione 

Downstream Products

• 157871-55-1 3-(4-pyridinyl)-5,6,7,8-tetrahydro-1,2,4-triazolo<4,3-a>pyrimidine 
• 123509-59-1 C₂₁H₂₂F₃N₆O⁽¹⁺⁾*2Br^(1-)*H⁽¹⁺⁾ 
• 123510-14-5 C₂₁H₂₅N₆O⁽¹⁺⁾*2Br^(1-)*H⁽¹⁺⁾ 
• 123509-45-5 C₂₁H₂₅N₆O⁽¹⁺⁾*2Br^(1-)*H⁽¹⁺⁾ 
• 123509-55-7 C₂₁H₂₅N₆O⁽¹⁺⁾*2Br^(1-)*H⁽¹⁺⁾ 
• 123540-46-5 C₂₂H₂₅N₆⁽¹⁺⁾*2Br^(1-)*H⁽¹⁺⁾ 
• 123509-71-7 C₂₂H₂₅N₆⁽¹⁺⁾*2Br^(1-)*H⁽¹⁺⁾ 
• 123510-17-8 C₁₈H₂₂N₅O⁽¹⁺⁾*2Br^(1-)*H⁽¹⁺⁾ 

Relevant articles and documents

Chloroacylhydrazones and chloroacylhydrazines of 1,3-diamines, part 1: Derivatives of 2-hydrazono-1,3-diamines as potential antitumor agents

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Synthesis and biological activity of mono- and bishydrazones of cyclic aminoguanidines

The paper reports the synthesis of hydrazones of five- and six-membered cyclic aminoguanidines with some aliphatic, aromatic and arylaliphatic ketones and the results of the studies on their antibacterial, antifungal and antiyeast activity.

2-(1,3-Diazacycloalkenyl)-2-hydrazones of substituted chalcones

The preparation of 2-(1,3-Diazacycloalkenyl)-2-hydrazones of substituted chalcones is described. These compounds are useful as anti-tubercular agents in warm-blooded animals.