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2-deoxy-2-[(2,4-dinitrophenyl)amino]hexopyranose is a complex organic compound with the molecular formula C12H16N4O8. It is a derivative of hexopyranose, a type of sugar molecule, where one of the hydroxyl groups (-OH) is replaced by an amino group (-NH2) attached to a 2,4-dinitrophenyl group. This modification results in a compound with unique chemical properties, making it potentially useful in various applications, such as in the study of carbohydrate chemistry, as a reagent in analytical chemistry, or as a building block for the synthesis of more complex molecules. The presence of the 2,4-dinitrophenyl group provides a distinct chromophore, which can be exploited for spectroscopic analysis or as a reporter group in biochemical assays.

7253-54-5

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7253-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7253-54-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7253-54:
(6*7)+(5*2)+(4*5)+(3*3)+(2*5)+(1*4)=95
95 % 10 = 5
So 7253-54-5 is a valid CAS Registry Number.

7253-54-5SDS

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-[(2,4-dinitrophenyl)amino]-6-(hydroxymethyl)oxane-2,4,5-triol

1.2 Other means of identification

Product number -
Other names N-(2,4-Dinitro-phenyl)-d-glucosamin

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:7253-54-5 SDS

7253-54-5Relevant academic research and scientific papers

Syntheses of N-aryl-protected glucosamines and their stereoselectivity in chemical glycosylations

Otsuka, Yuji,Yamamoto, Toshihiro,Fukase, Koichi

supporting information, p. 3019 - 3023 (2017/07/17)

N-Aryl-protecting groups were introduced in glucosamines to achieve β-selective glycosylation. Various N-aryl aminosugars were synthesized via Buchwald–Hartwig reaction. Glycosylation using glycosyl trichloroacetimidates of N-aryl aminosugars smoothly proceeded in the presence of trimethylsilyl trifluoromethanesulfonate. Use of a glycosyl donor comprising an electron-donating 2,4-dimethoxyphenyl (DMP) group led to the glycosylation proceeding with high β selectivity. This stereoselectivity seemed to be derived from the formation of an aziridine intermediate. The DMP-protecting group can be removed immediately by using ammonium hexanitratocerate (IV).

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