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2,4-dinitrophenyl 2,3,4,6-tetra-O-acetyl-1-thiohexopyranoside is a chemical compound derived from a thiohexopyranoside, a type of sugar molecule, and is modified with acetyl and dinitrophenyl groups. It is characterized by its ability to detect and quantify specific sugars in biological samples, making it a valuable tool in biochemical research.

3254-07-7

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3254-07-7 Usage

Uses

Used in Biochemical Research:
2,4-dinitrophenyl 2,3,4,6-tetra-O-acetyl-1-thiohexopyranoside is used as a detection and quantification agent for specific sugars in biological samples. The dinitrophenyl group allows for easy detection and measurement using spectrophotometric or chromatographic techniques, while the acetyl groups provide protection and stability to the sugar molecule, ensuring accurate and reliable analysis in a laboratory setting.
Used in Carbohydrate Analysis:
In the field of carbohydrate analysis, 2,4-dinitrophenyl 2,3,4,6-tetra-O-acetyl-1-thiohexopyranoside is employed as a labeling agent for sugars. Its unique structure enables the identification and quantification of various sugar molecules, contributing to a better understanding of their functions and interactions in biological systems.
Used in Pharmaceutical Development:
2,4-dinitrophenyl 2,3,4,6-tetra-O-acetyl-1-thiohexopyranoside may also be utilized in the development of pharmaceuticals targeting carbohydrate-related diseases. Its ability to detect and quantify specific sugars can aid in the discovery of potential drug candidates and the evaluation of their efficacy in modulating carbohydrate metabolism.
Used in Food Industry:
In the food industry, 2,4-dinitrophenyl 2,3,4,6-tetra-O-acetyl-1-thiohexopyranoside can be employed as an analytical tool for the detection and quantification of sugars in food products. This can help ensure product quality, monitor sugar content, and support the development of healthier food options.
Used in Environmental Science:
2,4-dinitrophenyl 2,3,4,6-tetra-O-acetyl-1-thiohexopyranoside can be applied in environmental science for the analysis of sugar content in environmental samples, such as soil, water, and plant materials. This can provide insights into the role of carbohydrates in ecosystem processes and help monitor the impact of human activities on natural sugar cycles.

Check Digit Verification of cas no

The CAS Registry Mumber 3254-07-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,5 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3254-07:
(6*3)+(5*2)+(4*5)+(3*4)+(2*0)+(1*7)=67
67 % 10 = 7
So 3254-07-7 is a valid CAS Registry Number.

3254-07-7SDS

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 [3,4,5-triacetyloxy-6-(2,4-dinitrophenyl)sulfanyloxan-2-yl]methyl acetate

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3254-07-7 SDS

3254-07-7Downstream Products

3254-07-7Relevant academic research and scientific papers

A general procedure for conversion of S-glycosyl isothiourea derivatives into thioglycosides, thiooligosaccharides and glycosyl thioesters

Ibatullin,Selivanov,Shavva

, p. 419 - 422 (2007/10/03)

A simple procedure for conversion of S-glycosyl isothiourea derivatives into thioglycosides by promotion with triethylamine is described. The reaction conditions allow the synthesis of glycosyl thioesters and some thioglycosides, which cannot be prepared using the traditional approach. The procedure has been successfully applied for preparation of thiooligosaccharides, shown by syntheses of methyl 4-thio-α-cellobioside and methyl 4-thio-α-lactoside derivatives.

Facile synthesis of 1,2-trans-nitrophenyl-1-thioglycopyranosides

Driguez,Szeja

, p. 1413 - 1414 (2007/10/02)

1,2-trans-2-Nitro-, 4-nitro- and 2,4-dinitrophenyl-1-thioglycopyranosides were synthesized in high yield by condensation of per-O-acetyl-1-thioglucose with the appropriate nitro- or dinitrofluorobenzene in the presence of potassium carbonate. The pseudothiourea precursor was also used under these coupling conditions. 1,2-trans-4-Nitrophenyl-1-thioglycosides derived from β-D-galactose, β-D-xylose, α-L-arabinose and maltose were also obtained in good yield.

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