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Methyl 3-deoxy-3-nitrohexopyranoside is a complex organic compound with the molecular formula C7H13NO6. It is a derivative of a hexopyranoside, which is a type of sugar molecule, where one of the hydroxyl groups has been replaced by a nitro group (-NO2) and another has been removed, resulting in a 3-deoxy (three oxygen atoms missing) structure. methyl 3-deoxy-3-nitrohexopyranoside is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and as a potential intermediate in the preparation of various pharmaceuticals and biologically active compounds. Its unique structure with a nitro group introduces new reactivity patterns, making it a valuable building block for the development of novel chemical entities.

4631-21-4

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4631-21-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4631-21-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,3 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4631-21:
(6*4)+(5*6)+(4*3)+(3*1)+(2*2)+(1*1)=74
74 % 10 = 4
So 4631-21-4 is a valid CAS Registry Number.

4631-21-4SDS

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 2-(hydroxymethyl)-6-methoxy-4-nitrooxane-3,5-diol

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

1.4 Supplier's details

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More Details:4631-21-4 SDS

4631-21-4Relevant academic research and scientific papers

A stereocontrolled synthesis of 3-acetamido-1,3,5-trideoxy- and 1,3,5,6-tetradeoxy-1,5-imino-d-glucitol

Simak, Ondrej,Stanek, Jan,Moravcova, Jitka

experimental part, p. 966 - 971 (2009/09/05)

3-Acetamido-5-amino-3,5,6-trideoxy-d-glucono-1,5-lactam and 3-acetamido-5-amino-3,5-dideoxy-d-glucono-1,5-lactam were synthesized from corresponding 3-acetamido-3-deoxy-β-d-glucopyranosides in 63% and 35% overall yield, respectively. Acetylation followed by reduction led to the title 3-acetamido-3-deoxy derivatives of both deoxynojirimycin and 1,6-dideoxynojirimycin. The procedure developed is useful for a multi-gram scale.

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