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1729-32-4

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1729-32-4 Usage

Derivative of furanone

A heterocyclic organic compound

Iodomethyl group

Suggests potential reactivity and chemical properties

Potentially toxic and hazardous

Should be handled with care and in accordance with safety guidelines and regulations

Uses and applications

Depend on further research and testing to determine its properties and potential uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1729-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1729-32:
(6*1)+(5*7)+(4*2)+(3*9)+(2*3)+(1*2)=84
84 % 10 = 4
So 1729-32-4 is a valid CAS Registry Number.

1729-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dihydro-5-(iodomethyl)furan-2(3H)-pne

1.2 Other means of identification

Product number -
Other names 5-iodomethyl-4,5-dihydrofuran-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:1729-32-4 SDS

1729-32-4Relevant articles and documents

An efficient chemoenzymatic approach to (S)-γ-fluoroleucine ethyl ester

Limanto, John,Shafiee, Ali,Devine, Paul N.,Upadhyay, Veena,Desmond, Richard A.,Foster, Bruce R.,Gauthier Jr., Donald R.,Reamer, Robert A.,Volante

, p. 2372 - 2375 (2007/10/03)

(Chemical Equation Presented) An asymmetric synthesis of (S)-γ-fluoroleucine ethyl ester 1 is described. The key transformation involves a lipase-catalyzed dynamic ring-opening of 2-(3-butenyl)azlactone 7b with EtOH to give amide ester (S)-6b in 84% enant

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