87487-96-5

Basic information

• Product Name: 3-AMINO-5-HYDROXY-PENTEN-1
• Synonyms: 3-AMINO-PENT-4-EN-1-OL;3-AMINO-5-HYDROXY-PENTEN-1;REF DUPL: 3-Amino-5-hydroxy-penten-1;1-Penten-3-ol, 5-amino-
• CAS NO: 87487-96-5
• Molecular Formula: C₅H₁₁NO
• Molecular Weight: 101.15
• Product Categories: pharmacetical
• Mol File: 87487-96-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-AMINO-5-HYDROXY-PENTEN-1(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-5-HYDROXY-PENTEN-1(87487-96-5)
• EPA Substance Registry System: 3-AMINO-5-HYDROXY-PENTEN-1(87487-96-5)

Safety Data

• Hazardous Substances Data: 87487-96-5(Hazardous Substances Data)

Usage

General Description

3-AMINO-5-HYDROXY-PENTEN-1 is a chemical compound with the molecular formula C5H11NO2. It is a pentenoic acid derivative with an amino group and a hydroxyl group attached to the carbon chain. 3-AMINO-5-HYDROXY-PENTEN-1 is known for its diverse chemical properties and has been identified as an intermediate in the biosynthesis of certain natural products. It is also used as a reagent in organic synthesis for the preparation of various pharmaceuticals and agricultural chemicals. Additionally, 3-AMINO-5-HYDROXY-PENTEN-1 has potential applications in the development of new materials and polymers due to its unique structural characteristics. Despite its relative novelty, ongoing research is exploring the full range of potential uses and implications of this compound in various fields.

Upstream product

• 27451-36-1 (RS)-3-hydroxypent-4-enenitrile 
• 87487-95-4 5-vinyl-2-isoxazoline 

Downstream Products

• 1256091-37-8 5-(N-benzylamino)pent-1-en-3-ol 
• 90778-63-5 N-(3-hydroxypent-4-enyl)-4-methylbenzenesulfonamide 
• 1345971-40-5 ethyl N-(3-t-butyldiphenylsilyloxy-4-pentenyl)carbamate 
• 144691-93-0 ethyl N-(3-hydroxy-4-pentenyl)carbamate 
• 108998-79-4 (2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(R)-1-hydroxy-2-((S)-2-hydroxy-1,2,2-triphenyl-ethoxycarbonyl)-ethyl]-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 108998-79-4 (2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(S)-1-hydroxy-2-((S)-2-hydroxy-1,2,2-triphenyl-ethoxycarbonyl)-ethyl]-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 98900-30-2 cis-2-hydroxymethyl-3-hydroxypyrrolidine hydrochloride 
• 126861-76-5 (2R,3R)-3-Hydroxy-2-hydroxymethyl-pyrrolidine-1-carboxylic acid benzyl ester 
• 126861-77-6 (2R,3R)-3-Hydroxy-2-methyl-pyrrolidine-1-carboxylic acid benzyl ester 
• 126861-75-4 N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine 

Relevant articles and documents

Continuous Pd-Catalyzed Carbonylative Cyclization Using Iron Pentacarbonyl as a CO Source

This work discloses a continuous flow carbonylation reaction using iron pentacarbonyl as source of CO. The described transformation using this surrogate was designed for use in commonly accessible flow equipment. Optimized conditions were applied to a sca

SILYL NITRONATES, NITRILE OXIDES, AND DERIVED 2-ISOXAZOLINES IN ORGANIC SYNTHESIS. FUNCTIONALIZATION OF BUTADIENE, A NOVEL ROUTE TO FURANS AND 2-ISOXAZOLINES AS AN ALTERNATIVE TO ALDOL-TYPE CONDENSATIONS

Mono- and di-addition of silylnitronates and nitrile oxides is a useful procedure for functionalizing butadiene leading to cyano and acyl derivatives.A novel route to 2,5-disubstituted furans is also established.The potential of the method in carbohydrate synthesis is pointed out.The route via 2-isoxazoline is shown to be a useful alternative to aldol-type reactions in organic synthesis. 15a has been studied by X-ray diffraction and shown to be meso form.