1245643-19-9

Basic information

• Product Name: (R)-N-(1,4-dihydroxybutan-2-yl)benzamide
• Synonyms: (R)-N-(1,4-dihydroxybutan-2-yl)benzamide
• CAS NO: 1245643-19-9
• Molecular Formula: C11H15NO3
• Molecular Weight: 209.2417
• Mol File: 1245643-19-9.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (R)-N-(1,4-dihydroxybutan-2-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-N-(1,4-dihydroxybutan-2-yl)benzamide(1245643-19-9)
• EPA Substance Registry System: (R)-N-(1,4-dihydroxybutan-2-yl)benzamide(1245643-19-9)

Safety Data

• Hazardous Substances Data: 1245643-19-9(Hazardous Substances Data)

Usage

General Description

(R)-N-(1,4-dihydroxybutan-2-yl)benzamide is a chemical compound with the molecular formula C14H17NO3. It is a derivative of benzamide and contains a butan-2-yl group attached to the nitrogen atom. The compound also contains two hydroxyl groups attached to the butan-2-yl group at the first and fourth carbon atoms. This chemical is used in various pharmaceutical and organic synthesis applications due to its unique structure and potential biological activities. It may be used in the development of new drugs or as a research tool in biochemical studies.

Upstream product

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

Downstream Products

• 864954-12-1 (2S,5S)-2-(p-aminophenyl)-5-benzoylamino-1,3-dioxapane 
• 152495-79-9 (S)-3-benzoylamino-tetrahydrofuran 

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.

5-Benzoylamino-1,3-dioxacyclanes, the method for preparing the same and their use as PKC inhibitor

The present invention discloses a series of benzoylamino-1,3-dioxacyclane compounds, of which compounds 1-21 were prepared via transacetalisation reaction between N-benzoylaminoglycol and 1,1,3,3-tetramethoxypropane; while compounds 22-48 were prepared vi