17435-30-2

Basic information

• Product Name: (R)-1-((5-aMino-6-chloropyriMidin-4-yl)aMino)propan-2-ol
• Synonyms: (R)-1-((5-aMino-6-chloropyriMidin-4-yl)aMino)propan-2-ol
• CAS NO: 17435-30-2
• Molecular Formula: C7H11ClN4O
• Molecular Weight: 202.64144
• Mol File: 17435-30-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (R)-1-((5-aMino-6-chloropyriMidin-4-yl)aMino)propan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-((5-aMino-6-chloropyriMidin-4-yl)aMino)propan-2-ol(17435-30-2)
• EPA Substance Registry System: (R)-1-((5-aMino-6-chloropyriMidin-4-yl)aMino)propan-2-ol(17435-30-2)

Safety Data

• Hazardous Substances Data: 17435-30-2(Hazardous Substances Data)

Usage

General Description

(R)-1-((5-amino-6-chloropyrimidin-4-yl)amino)propan-2-ol is a chemical compound with the chemical formula C8H14ClN5O. It is a derivative of pyrimidine and is commonly used in the pharmaceutical industry as an antiviral agent. (R)-1-((5-aMino-6-chloropyriMidin-4-yl)aMino)propan-2-ol is known to inhibit the replication of viruses, particularly those that belong to the herpes virus family. Its mode of action involves interfering with the viral DNA synthesis, thus preventing the virus from replicating and spreading within the host. This makes it an important component in the development of antiviral drugs and medications. Additionally, it has also been studied for its potential use in treating certain types of cancer, due to its ability to inhibit DNA synthesis in rapidly dividing cells.

Upstream product

• 5413-85-4 5-amino-4,6-dichloropyridimine 
• 2799-16-8 (2R)-hydroxypropylamine 

Downstream Products

• 180587-75-1 (R)-diethyl (((1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonate 
• 147127-20-6 tenofovir 
• 14047-28-0 (R)-9-(2-hydroxypropyl)adenine 
• 180587-74-0 (R)-1-(6-chloro-9H-purin-9-yl) propan-2-ol 

Relevant articles and documents

Kinetic resolution of terminal epoxides via highly regioselective and enantioselective ring opening with TMSN3. An efficient, catalytic route to 1,2-amino alcohols

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