296766-73-9

Basic information

• Product Name: (S)-N-(1,4-dihydroxybutan-2-yl)benzamide
• Synonyms: (S)-N-(1,4-dihydroxybutan-2-yl)benzamide;N-[(2S)-1,4-dihydroxybutan-2-yl]benzamide
• CAS NO: 296766-73-9
• Molecular Formula: C₁₁H₁₅NO₃
• Molecular Weight: 209.2417
• Mol File: 296766-73-9.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (S)-N-(1,4-dihydroxybutan-2-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(1,4-dihydroxybutan-2-yl)benzamide(296766-73-9)
• EPA Substance Registry System: (S)-N-(1,4-dihydroxybutan-2-yl)benzamide(296766-73-9)

Safety Data

• Hazardous Substances Data: 296766-73-9(Hazardous Substances Data)

Usage

General Description

(S)-N-(1,4-dihydroxybutan-2-yl)benzamide is a chemical compound with the molecular formula C13H17NO3. It is a derivative of benzamide and contains a butan-2-yl group with two hydroxyl (OH) functional groups attached to the carbon chain. (S)-N-(1,4-dihydroxybutan-2-yl)benzamide is a chiral molecule, meaning it exists as two enantiomers, (S)-N-(1,4-dihydroxybutan-2-yl)benzamide and (R)-N-(1,4-dihydroxybutan-2-yl)benzamide, which are mirror images of each other. The compound may have potential applications in pharmaceuticals and medicinal chemistry, and its properties and uses could be further investigated.

Upstream product

• 86555-45-5 (2S)-N-benzoyl-L-aspartic acid dimethyl ester 
• 98-88-4 benzoyl chloride 
• 40856-55-1 (S)-2-benzoylamino-γ-butyrolactone 
• 82933-21-9 N-benzoyl-L-aspartic acid α-methyl ester 

Downstream Products

• 296766-52-4 N-[(2R,5S)-2-(2,2-dimethoxyethyl)-1,3-dioxacycloheptan-5-yl]benzoylamine 
• 152495-79-9 (S)-3-benzoylamino-tetrahydrofuran 
• 864954-12-1 (2S,5S)-2-(p-aminophenyl)-5-benzoylamino-1,3-dioxapane 

Relevant articles and documents

Expeditious novel routes to enantiopure 3-amino tetrahydrofuran hydrochloride

The synthesis of chemically and enantiomerically pure (S)-3-amino tetrahydrofuran hydrochloride starting from the natural amino acids, l-aspartic acid or l-methionine is described. The process involves no chromatography and can be easily carried out on a large scale. The enantiopurity of the final product was established by NMR and chiral HPLC methods.

Processes for the Manufacture of Chiral and Racemic Forms of 3-Aminotetrahydrofurans, Their Salts and Derivatives

A novel process for the synthesis of (S)-3-Amino-tetrahydrofuran and (R)-3-Amino-tetrahydrofuran is described. The process is applicable for substituted chiral-3-aminotetrahydrofuran derivatives.

Modular chiral selenium-containing oxazolines: Synthesis and application in the palladium-catalyzed asymmetric allylic alkylation

A new series of modular chiral selenium-containing oxazolines has been synthesized from inexpensive and commercially available l-serine and l-aspartic acid. These new compounds were evaluated as chiral ligands in the palladium-catalyzed asymmetric allylic