873409-32-6

Basic information

• Product Name: 2-Amino-5-benzyl-4-hydroxypyrimidine
• Synonyms: 2-Amino-5-benzyl-4-hydroxypyrimidine;4-Pyrimidinol,2-amino-5-benzyl-(5CI);2-aMino-5-benzylpyriMidin-4(3H)-one
• CAS NO: 873409-32-6
• Molecular Formula: C₁₁H₁₁N₃O
• Molecular Weight: 201.22454
• Product Categories: VARIOUSAMINE
• Mol File: 873409-32-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Density: 1.28g/cm³
• Refractive Index: 1.65
• CAS DataBase Reference: 2-Amino-5-benzyl-4-hydroxypyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-5-benzyl-4-hydroxypyrimidine(873409-32-6)
• EPA Substance Registry System: 2-Amino-5-benzyl-4-hydroxypyrimidine(873409-32-6)

Safety Data

• Hazardous Substances Data: 873409-32-6(Hazardous Substances Data)

Usage

Description

2-Amino-5-benzyl-4-hydroxypyrimidine is a pyrimidine derivative with the molecular formula C12H12N4O. It features an amino group at the 2-position, a benzyl group at the 5-position, and a hydroxyl group at the 4-position. 2-Amino-5-benzyl-4-hydroxypyrimidine is not extensively studied or utilized, but its unique structure and the biological activity of pyrimidine derivatives suggest potential applications in medicinal chemistry and chemical synthesis.

Uses

Used in Medicinal Chemistry:
2-Amino-5-benzyl-4-hydroxypyrimidine is used as a potential candidate for drug development due to its structural features and the known biological activity of pyrimidine derivatives. Its presence in many pharmaceutical compounds highlights its significance in creating new therapeutic agents.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-Amino-5-benzyl-4-hydroxypyrimidine may serve as a building block or intermediate for synthesizing more complex molecules with specific applications. Its unique functional groups can be utilized in various chemical reactions to create a range of products.
Further research into the properties and potential uses of 2-Amino-5-benzyl-4-hydroxypyrimidine is necessary to fully understand its role and significance in chemical and medicinal applications.

InChI:InChI=1/C11H11N3O/c12-11-13-7-9(10(15)14-11)6-8-4-2-1-3-5-8/h1-5,7H,6H2,(H3,12,13,14,15)

Upstream product

• 1247016-07-4 6-benzyl-[1,2,3,4]tetrazolo[1,5-a]pyrimidin-7(4H)-one 
• 1247015-99-1 2-azido-5-benzylpyrimidin-4(3H)-one 
• 98516-80-4 ethyl 2-formyl-3-phenylpropionate 
• 50-01-1 guanidine hydrochloride 

Downstream Products

• 69945-52-4 5-(4-Nitro-benzyl)-pyrimidine-2,4-diamine 
• 259683-41-5 5-benzyl-4-chloro-pyrimidin-2-ylamine 
• 7319-45-1 2,4-diamino-5-benzylpyrimidine 

Relevant articles and documents

Application of primary allylamines from morita-baylis-hillman adducts: Cyanogen azide mediated synthesis of substituted 5-aminotetrazoles and their attempted transformation into tetrazolo[1,5-a]pyrimidinones

A general protocol for the synthesis of substituted 5-aminotetrazoles by treating cyanogen azide with primary allylamines afforded either by S N2 or SN2′ reactions of Morita- Baylis-Hillman acetates of acrylate has been developed. Th