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Methyl 3-(acetylamino)-3-deoxy-α-D-glucopyranoside 2,4,6-triacetate is a complex organic compound with the molecular formula C14H21NO8. It is a derivative of a sugar molecule, specifically a glucopyranoside, which has been modified with acetylamino and acetate groups. The compound features a methyl group attached to the 3-position of the glucopyranoside ring, with an acetylamino group also at the 3-position. Additionally, the 2, 4, and 6 positions of the ring are each substituted with an acetate group. This chemical is significant in the field of organic chemistry, particularly in the synthesis of complex carbohydrates and as a potential intermediate in the preparation of various pharmaceuticals and biologically active compounds. Its structure and properties make it a subject of interest for researchers studying the chemistry of carbohydrates and their applications in medicine and biochemistry.

2595-38-2

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2595-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2595-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2595-38:
(6*2)+(5*5)+(4*9)+(3*5)+(2*3)+(1*8)=102
102 % 10 = 2
So 2595-38-2 is a valid CAS Registry Number.

2595-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl-(tri-O-acetyl-3-acetylamino-3-deoxy-α-D-glucopyranoside)

1.2 Other means of identification

Product number -
Other names Methyl-(tri-O-acetyl-3-acetylamino-3-desoxy-α-D-glucopyranosid)

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:2595-38-2 SDS

2595-38-2Downstream Products

2595-38-2Relevant academic research and scientific papers

Stereoselective Protection-Free Modification of 3-Keto-saccharides

Bianca, Simona,Duca, Margherita,Marinus, Nittert,Minnaard, Adriaan J.,Mouthaan, L. M. C. Marc,Poolman, Bert,Tahiri, Nabil,Van Den Noort, Marco,Witte, Martin D.

supporting information, (2020/07/24)

Unprotected 3-keto-saccharides have become readily accessible via site-selective oxidation, but their protection-free functionalization is relatively unexplored. Here we show that protecting groups are obsolete in a variety of stereoselective modifications of our model substrate methyl α-glucopyranoside. This allows the preparation of rare sugars and the installation of click handles and reactive groups. To showcase the applicability of the methodology, maltoheptaose has been converted into a chemical probe, and the rare sugar evalose has been synthesized.

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