263870-93-5

Basic information

• Product Name: (S)-2-Amino-4-penten-1-ol
• Synonyms: (S)-2-Amino-4-penten-1-ol;(2S)-2-AMINOPENT-4-EN-1-OL;(S)-2-aminopent-4-en-1-ol;(2S)-allylglycinol
• CAS NO: 263870-93-5
• Molecular Formula: C₅H₁₁NO
• Molecular Weight: 101.14694
• Mol File: 263870-93-5.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 192.4±28.0 °C(Predicted)
• Appearance: /
• Density: 0.938±0.06 g/cm3(Predicted)
• PKA: 12.79±0.10(Predicted)
• CAS DataBase Reference: (S)-2-Amino-4-penten-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-Amino-4-penten-1-ol(263870-93-5)
• EPA Substance Registry System: (S)-2-Amino-4-penten-1-ol(263870-93-5)

Safety Data

• Hazardous Substances Data: 263870-93-5(Hazardous Substances Data)

Usage

Description

(S)-2-Amino-4-penten-1-ol, also known as L-2-amino-4-penten-1-ol or 2-amino-4-penten-1-ol, is a colorless liquid chemical compound with the molecular formula C5H11NO. It is characterized by an amine odor and is recognized as a chiral, non-proteinogenic amino alcohol. (S)-2-Amino-4-penten-1-ol is highly valued in the field of organic chemistry and chemical synthesis due to its stereochemistry, which enables its use in asymmetric synthesis, and its role as an important intermediate in the creation of various complex organic molecules.

Uses

Used in Pharmaceutical Synthesis:
(S)-2-Amino-4-penten-1-ol is used as a chiral building block for the synthesis of pharmaceuticals. Its unique stereochemistry allows for the creation of complex organic molecules that are essential in the development of new drugs and medications.
Used in Agrochemical Production:
(S)-2-Amino-4-penten-1-ol is also utilized in the production of agrochemicals, which are chemicals specifically designed to benefit crop or livestock production, such as pesticides, fertilizers, and other agricultural aids.
Used in Fragrance and Flavor Industries:
(S)-2-Amino-4-penten-1-ol is employed in the creation of fragrances and flavors, where its unique properties contribute to the development of novel and distinct scents and tastes for various consumer products.
Used in Asymmetric Synthesis:
Due to its stereochemistry, (S)-2-Amino-4-penten-1-ol is a valuable intermediate in asymmetric synthesis, a technique that allows for the selective production of one enantiomer of a molecule over another. This selective synthesis is crucial in the development of enantiomerically pure compounds, which can have different biological activities and properties.

Upstream product

• 16338-48-0 L-allylglycine 
• 1388191-48-7 C₁₅H₃₃NO₂SSi 
• 173723-62-1 (S)-allylglycine methyl ester hydrochloride 

Downstream Products

• 1388191-54-5 C₁₈H₃₁NOSi 
• 1388191-43-2 C₂₀H₃₂N₂OSi 
• 174626-20-1 benzyl (S)-(1-hydroxypent-4-en-2-yl)carbamate 
• 263871-10-9 (5R,7S,8aS)-5-Benzyl-6-hydroxy-3,3,7-trimethyl-4-oxo-hexahydro-2-oxa-3a,6-diaza-azulene-7-carbonitrile 
• 263871-02-9 (7R,8aS)-5-Benzyl-3,3,7-trimethyl-4-oxo-4,7,8,8a-tetrahydro-1H-2-oxa-3a,6-diaza-azulene-7-carbonitrile 

Relevant articles and documents

FUSED TRICYCLIC HETEROCYCLE COMPOUNDS AND THERAPEUTIC USES THEREOF

This application discloses a new class of fused tricyclic heterocycles of formula (I), preparation methods thereof, pharmaceutical compositions comprising these compounds, and pharmaceutically acceptable salts, solvates, or prodrugs thereof, and their use

Two phenyls are better than one or three: Synthesis and application of terminal olefin-oxazoline (TOlefOx) ligands

A novel terminal olefin-oxazoline ligand was introduced into rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to enones and gave excellent enantioselectivities. The two phenyls proved better than one or three in ligand evaluations.

AZABICYCLO [4.1.0] HEPT - 4 - YL DERIVATIVES AS HUMAN OREXIN RECEPTOR ANTAGONISTS

This invention relates to azabicyclo[4.1.0]hept-4-yl derivatives and their use as pharmaceuticals.