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Methyl 2,3,4-tri-O-acetyl-6-deoxy-6-nitrohexopyranoside is a complex organic compound with the molecular formula C12H15NO9. It is a derivative of a hexopyranoside, which is a type of sugar molecule, specifically a hexose (six-carbon sugar). In methyl 2,3,4-tri-O-acetyl-6-deoxy-6-nitrohexopyranoside, three hydroxyl groups (-OH) at the 2, 3, and 4 positions are acetylated, meaning they are replaced by acetate groups (-COCH3). Additionally, the 6-position is deoxygenated (lacking an oxygen atom) and nitrated (substituted with a nitro group, -NO2). This chemical is often used as an intermediate in the synthesis of various complex carbohydrates and pharmaceuticals, particularly those with modified sugar moieties. Its unique structure allows for further chemical modifications, making it a valuable building block in organic synthesis.

4969-34-0

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4969-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4969-34-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4969-34:
(6*4)+(5*9)+(4*6)+(3*9)+(2*3)+(1*4)=130
130 % 10 = 0
So 4969-34-0 is a valid CAS Registry Number.

4969-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [4,5-diacetyloxy-6-methoxy-2-(nitromethyl)oxan-3-yl] acetate

1.2 Other means of identification

Product number -
Other names methyl 2,3,4-tri-O-acetyl-6-deoxy-6-nitrohexopyranoside

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:4969-34-0 SDS

4969-34-0Downstream Products

4969-34-0Relevant academic research and scientific papers

Method for preparing 6-nitro-deoxy-triacetylmethyl glucoside

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Paragraph 0010; 0023-0024, (2017/09/12)

The invention discloses a method for preparing 6-nitro-deoxy-triacetylmethyl glucoside. The method comprises the following steps: S1, by taking methyl glucoside as the raw material, directly performing iodination on six primary hydroxyl groups of methyl glucoside by use of iodine, triphenylphosphine and imidazole to prepare 6-iodomethyl glucoside; S2, protecting a hydroxyl group of 6-iodomethyl glucoside by use of an acetyl group; and S3, enabling reaction between the product of S2 and sodium nitrite and phloroglucinol to obtain the target product. Physical parameters of the obtained product are consistent with descriptions of documents, and the structure is confirmed by nuclear magnetic resonance hydrogen spectrometry and nuclear magnetic resonance mass spectrometry. The method is simple and feasible in route, silica gel column chromatography is not needed after finish of each step of reaction, and the method is suitable for not only mini-preparation in a laboratory for scientific research but also industrial production amplification, and is high in efficiency and low in cost.

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