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5406-65-5

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5406-65-5 Usage

General Description

Ethyl 5-(chloromethyl)-2-oxotetrahydrofuran-3-carboxylate is a chemical compound with the molecular formula C9H13ClO4. It is an ester derivative of tetrahydrofuran and is commonly used as a reagent in organic synthesis. It is a colorless liquid with a faint, sweet odor and is highly flammable. ethyl 5-(chloromethyl)-2-oxotetrahydrofuran-3-carboxylate is known to be an intermediate in the synthesis of pharmaceuticals and agrochemicals. The chloromethyl group in this compound makes it reactive and useful in various organic reactions, making it a valuable chemical in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 5406-65-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5406-65:
(6*5)+(5*4)+(4*0)+(3*6)+(2*6)+(1*5)=85
85 % 10 = 5
So 5406-65-5 is a valid CAS Registry Number.

5406-65-5SDS

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 ethyl 5-(chloromethyl)-2-oxooxolane-3-carboxylate

1.2 Other means of identification

Product number -
Other names 5-chloromethyl-2-oxo-tetrahydro-furan-3-carboxylic acid ethyl ester

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:5406-65-5 SDS

5406-65-5Downstream Products

5406-65-5Relevant articles and documents

Five membered ring formation of 2-hydroxyalkyl malonate and acetoacetate derivatives the problem of O-versus C-alkylation

Adams, Elisabeth,Hiegemann, Monika,Duddeck, Helmut,Welzel, Peter

, p. 5975 - 5992 (2007/10/02)

The cyclization reactions of type 32, 34, 36, 37/38 compounds have been studied with the aim of achieving a carbon-carbon bond forming reaction at C-2 of optically active glycerol derivatives as indicated in Scheme 1. In all cases O-alkylation at the proximal CO group has been observed.

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