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2(5H)-Furanone, 5-hydroxy-5-(methoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110339-35-0

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110339-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110339-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,3,3 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110339-35:
(8*1)+(7*1)+(6*0)+(5*3)+(4*3)+(3*9)+(2*3)+(1*5)=80
80 % 10 = 0
So 110339-35-0 is a valid CAS Registry Number.

110339-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-5-(methoxymethyl)furan-2-one

1.2 Other means of identification

Product number -
Other names 5-hydroxy-5-(methoxymethyl)furan-2(5H)-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:110339-35-0 SDS

110339-35-0Downstream Products

110339-35-0Relevant academic research and scientific papers

Photo-oxygenation des derives de l'hydroxymethyl-5 furfural-2

Cottier, Louis,Descotes, Gerard,Nigay, Henri,Parron, Jean-Claude,Gregoire, Veronique

, p. 844 - 850 (2007/10/02)

Photosensitized oxygenations in alcoholic solution of the furfural compounds 1,6-9 and the furanic compounds 10-17 yield the hydroxybutenolides 2a, 1, 20, 21, 22, the alkoxybutenolides 5, 19, 23, 24 and the unsaturated compounds 25 and 26.With rose bengal fixed on the polysaccharide resin Sephadex A 25 as sensitizer, the quantum yields of singlet oxygen formation in methanol or ethanol are higher (19 to 116percent) than those obtained with the commercial resin Sensitox.Kinetic results for these photo-oxygenations show the electronic influence of the substitution on C2 or C5.Depending on these substituants, several reaction pathways can be envisaged in order to explain the formation of the products.

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