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Methyl 2,3-anhydropentofuranoside is a chemical compound with the molecular formula C6H10O4. It is a derivative of pentofuranose, a type of sugar molecule, where the 2nd and 3rd hydroxyl groups are connected through an anhydro bridge, and a methyl group is attached to the oxygen atom. methyl 2,3-anhydropentofuranoside is significant in organic chemistry and carbohydrate chemistry, as it represents a structural motif found in various natural products and can be used as a building block for the synthesis of more complex molecules. Its anhydro structure and methyl substitution contribute to its unique reactivity and potential applications in the development of pharmaceuticals and other bioactive compounds.

4860-82-6

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4860-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4860-82-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4860-82:
(6*4)+(5*8)+(4*6)+(3*0)+(2*8)+(1*2)=106
106 % 10 = 6
So 4860-82-6 is a valid CAS Registry Number.

4860-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2,3-4,5-di-O-isopropylidine-glucoseptanoside

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:4860-82-6 SDS

4860-82-6Relevant academic research and scientific papers

An efficient synthesis of methyl 2,3-anhydro-α-D-ribofuranoside

Callam, Christopher S.,Gadikota, Rajendrakumar Reddy,Lowary, Todd L.

, p. 267 - 270 (2007/10/03)

An efficient synthesis of methyl 2,3-anhydro-α-D-ribofuranoside is reported. Its preparation is achieved via a four-step sequence from methyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranoside in 74% overall yield.

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