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5-(Arabino-tetrahydroxybutyl)-2-methyl-3-furoic acid is a complex organic compound with the molecular formula C10H16O7. It is a derivative of 3-furoic acid, featuring a methyl group at the 2-position and a unique arabino-tetrahydroxybutyl side chain at the 5-position. This side chain consists of a butane backbone with four hydroxyl groups attached, giving the molecule its distinctive structure. The compound is known for its potential applications in various fields, including pharmaceuticals and chemical research, due to its unique chemical properties and reactivity. Its specific role and effectiveness in these applications are subjects of ongoing study and experimentation.

3351-43-7

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3351-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3351-43-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3351-43:
(6*3)+(5*3)+(4*5)+(3*1)+(2*4)+(1*3)=67
67 % 10 = 7
So 3351-43-7 is a valid CAS Registry Number.

3351-43-7SDS

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 2-methyl-5-[(1S,2R,3R)-1,2,3,4-tetrahydroxybutyl]-3-furoate

1.2 Other means of identification

Product number -
Other names 3-ethoxycarbonyl-5-(D-arabino-tetrahydroxybutyl)-2-methylfuran

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:3351-43-7 SDS

3351-43-7Relevant academic research and scientific papers

Synthesis and biological evaluation of modified 2-deoxystreptamine dimers

Coste, Gerald,Horlacher, Tim,Molina, Lidia,Moreno-Vargas, Antonio J.,Carmona, Ana T.,Robina, Inmaculada,Seeberger, Peter H.,Gerber-Lemaire, Sandrine

experimental part, p. 1759 - 1770 (2011/07/30)

Aminoglycosides are powerful antibiotics, but the emergence of resistant bacterial strains has prompted the search for analogues with better pharmacological profiles. The synthesis of 2-deoxystreptamine (2-DOS) dimers linked by polyamines and analogues based on furylcarbopeptoid skeletons is described. Potent and selective ligands for bacterial 16S rRNA were identified using microarray techniques by determining the affinity of these derivatives toward bacterial and human ribosomal RNAs. Georg Thieme Verlag Stuttgart - New York.

"Furan endwise peeling" of celluloses: Mechanistic studies and application perspectives of a novel reaction

Yoneda, Yuko,Krainz, Karin,Liebner, Falk,Potthast, Antje,Rosenau, Thomas,Karakawa, Makoto,Nakatsubo, Fumiaki

, p. 475 - 484 (2008/09/18)

The mechanism of a novel reaction type, the "furan endwise peeling" reaction, has been studied. Making extensive use of experiments on model compounds, the structural prerequisites to the reaction were found to be a 2-hydroxpyran β-glycosidically linked t

SiO2-supported CeCl3·7H2O-NaI Lewis acid promoter: Investigation into the Garcia Gonzalez reaction in solvent-free conditions

Bartoli, Giuseppe,Fernandez-Bolanos, Jose G.,Di Antonio, Giustino,Foglia, Gioia,Giuli, Sandra,Gunnella, Roberto,Mancinelli, Michele,Marcantoni, Enrico,Paoletti, Melissa

, p. 6029 - 6036 (2008/02/10)

(Chemical Equation Presented) The Knoevenagel condensation of aldose sugars with β-dicarbonyl compounds produces furan derivatives having polyhydroxyalkylated alkyl side chains; this reaction is known as the Garcia Gonzalez reaction. Despite the fact that

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