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"2(3H)-Furanone, 5-(azidomethyl)dihydro-, (S)-" is a complex organic chemical compound with the molecular formula C5H7N3O2. It is a derivative of dihydrofuranone, featuring an azido group (N3) attached to a methylene (CH2) bridge, which in turn is connected to the furanone ring. The "S" notation indicates that the compound has a specific stereochemistry, with the azido group positioned on the left side when the molecule is oriented in a standard manner. 2(3H)-Furanone, 5-(azidomethyl)dihydro-, (S)- is of interest in organic synthesis and may have potential applications in the development of pharmaceuticals or other specialty chemicals due to its unique structure and reactivity.

24211-53-8

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24211-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24211-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,1 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24211-53:
(7*2)+(6*4)+(5*2)+(4*1)+(3*1)+(2*5)+(1*3)=68
68 % 10 = 8
So 24211-53-8 is a valid CAS Registry Number.

24211-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(+)-5-Azidomethyl-2-oxotetrahydrofuran

1.2 Other means of identification

Product number -
Other names (5S)-5-(azidomethyl)oxolan-2-one

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:24211-53-8 SDS

24211-53-8Relevant academic research and scientific papers

Concise Enantioselective Synthesis of Naturally Active (S)-3-Hydroxypiperidine

Dey, Soumen,Karabal, Pratibha U.,Sudalai, Arumugam

, p. 1559 - 1565 (2015/06/02)

A short and efficient enantioselective synthesis of natural product (S)-3-hydroxypiperidine has been achieved starting from commercially available raw materials employing two catalytic routes: (i) cocatalyzed hydrolytic kinetic resolution (HKR) of racemic methyl-3-(oxiran-2-yl)propanoate; (ii) proline-catalyzed α-aminooxylation followed by Horner-Wardsworth-Emmons olefination in high enantiomeric purity (97% ee) and high overall yield (38%). (Chemical Equation Presented).

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