40808-62-6

Basic information

• Product Name: RARECHEM AN KA 0161
• Synonyms: RARECHEM AN KA 0161;2-(1H-PYRROL-2-YL)-ETHYLAMINE;2-(1H-PYRROL-2-YL)-ETHYLAMINE HYDROCHLORIDE;2-(2-Pyrrolyl)ethylamine;2-(2-AMinoethyl)pyrrole;1H-Pyrrole-2-ethanamine;3-(1H-pyrrol-2-yl)propan-1-amine
• CAS NO: 40808-62-6
• Molecular Formula: C₆H₁₀N₂
• Molecular Weight: 110.16
• Mol File: 40808-62-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 229℃
• Flash Point: 115℃
• Appearance: /
• Density: 1.056
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 17.44±0.50(Predicted)
• CAS DataBase Reference: RARECHEM AN KA 0161(CAS DataBase Reference)
• NIST Chemistry Reference: RARECHEM AN KA 0161(40808-62-6)
• EPA Substance Registry System: RARECHEM AN KA 0161(40808-62-6)

Safety Data

• Hazardous Substances Data: 40808-62-6(Hazardous Substances Data)

Usage

General Description

RARECHEM AN KA 0161 is a chemical substance that is also known by its chemical name, 1-((2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl)gua- nine. It is a rare chemical compound with potential pharmaceutical and research applications. It is a guanine derivative with a furanose sugar moiety that has been identified as a component in certain natural products. Further research and study may be needed to fully understand its properties and potential uses in various industries.

Upstream product

• 50551-29-6 2-pyrroleacetonitrile 
• 89532-48-9 Pyrrol-2-acetamid 
• 86688-93-9 1-benzenesulfonyl-2-formylpyrrole 
• 14745-84-7 2-(N,N-dimethylaminomethyl)pyrrole 
• 4778-25-0 (1H-pyrrol-2-yl)acetic acid ethyl ester 
• 72607-07-9 2-(2-nitrovinyl)pyrrole 
• 1003-29-8 2-pyrrole aldehyde 
• 276239-25-9 2-[(E)-2-nitroeth-1-enyl]-1H-pyrrole 

Downstream Products

• 855263-47-7 N-(2-pyrrol-2-yl-ethyl)-benzamide 
• 82859-02-7 4-carbethoxymethyl-4,5,6,7-tetrahydro<1H>pyrrolo<3,2-c>pyridine 
• 860362-26-1 4-methylpyrrolo[3,2-c]pyridine 
• 860721-07-9 4-phenyl-6,7-dihydro-1H-pyrrolo[3,2-c]pyridine 
• 1623752-27-1 benzyl (2-(1H-pyrrol-2-yl)ethyl)carbamate 
• 942077-76-1 (2-pyrrolidin-1-ylethyl)carbamic acid tert-butyl ester 

Relevant articles and documents

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An Enantio- and Diastereoselective Mannich/Pictet–Spengler Sequence To Form Spiro[piperidine-pyridoindoles] and Application to Library Synthesis

A new tandem strategy based on a Mannich/Pictet–Spengler sequence has been developed and applied to the synthesis of a new small library (14 examples) of privileged compounds based on the spiro[piperidine-pyridoindole] core. The sequence proceeds by a diastereoselective Pictet–Spengler cyclization after condensation of several tryptamine derivatives with three novel piperidin-4-ones containing the fluorinated substituents F, CF3and SF5. The piperidin-4-ones were synthesized from readily available starting materials by an enantioselective multi-component organocatalytic Mannich reaction.

Synthesis of β-pyrrolalkylamines

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