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152495-79-9

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152495-79-9 Usage

General Description

(R)-N-(tetrahydrofuran-3-yl)benzamide is a chemical compound characterized by a benzene ring linked to a tetrahydrofuran group and an amide functional group. The compound is chiral, with a specific three-dimensional arrangement of its atoms, denoted as (R). It is commonly used in the pharmaceutical industry for its potential as a building block in organic synthesis and drug development. Its unique structure and properties make it a valuable tool for chemists and researchers working in the field of medicinal chemistry, and it has shown promise in various biological studies and drug discovery efforts. Additionally, the compound may also have potential applications in other industrial and scientific areas.

Check Digit Verification of cas no

The CAS Registry Mumber 152495-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,4,9 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 152495-79:
(8*1)+(7*5)+(6*2)+(5*4)+(4*9)+(3*5)+(2*7)+(1*9)=149
149 % 10 = 9
So 152495-79-9 is a valid CAS Registry Number.

152495-79-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(3R)-oxolan-3-yl]benzamide

1.2 Other means of identification

Product number -
Other names (R)-N-(tetrahydrofuran-3-yl)benzamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:152495-79-9 SDS

152495-79-9Relevant articles and documents

Expeditious novel routes to enantiopure 3-amino tetrahydrofuran hydrochloride

Ramanujam, Rajendran,Ganjihal, Savita,Kalyanam, Nagabushanam,Majeed, Muhammed

, p. 663 - 668 (2013/07/11)

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.

A Remarkable Base-Induced Rearrangement of Hydroxy Oxazolines to Amido Tetrahydrofurans

Wilson, Kenneth J.,Sabat, Michal,McGarvey, Glenn J.

, p. 6180 - 6181 (2007/10/02)

Asymmetric β-hydroxy oxazolines heve been shown to rearrange at room temperature to isomeric tetrahydrofurans when deprotonated with potassium hydride in tetrahydrofuran.

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