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1,3,4-tri-O-acetyl-2-(acetylamino)-2-deoxy-6-O-tritylhexopyranose is a carbohydrate derivative belonging to the hexopyranose family. It features three acetyl groups at positions 1, 3, and 4, an acetylamino group at position 2, and a trityl group at position 6. 1,3,4-tri-O-acetyl-2-(acetylamino)-2-deoxy-6-O-tritylhexopyranose is widely used in organic synthesis, particularly for the production of complex molecules such as glycosides and glycopeptides. It also plays a significant role in the study of carbohydrate chemistry and serves as a building block for synthesizing various biologically active compounds. Furthermore, it has potential applications in the development of pharmaceuticals and bioconjugates.

10026-54-7

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10026-54-7 Usage

Uses

Used in Organic Synthesis:
1,3,4-tri-O-acetyl-2-(acetylamino)-2-deoxy-6-O-tritylhexopyranose is used as a key intermediate in the synthesis of complex molecules such as glycosides and glycopeptides. Its unique structure allows for the formation of various derivatives, making it a valuable component in organic synthesis.
Used in Carbohydrate Chemistry Research:
1,3,4-tri-O-acetyl-2-(acetylamino)-2-deoxy-6-O-tritylhexopyranose is utilized in the study of carbohydrate chemistry, providing insights into the structure, properties, and reactions of carbohydrates. It serves as a model compound for understanding the behavior of similar carbohydrate derivatives and contributes to the advancement of carbohydrate chemistry.
Used in Pharmaceutical Development:
1,3,4-tri-O-acetyl-2-(acetylamino)-2-deoxy-6-O-tritylhexopyranose has potential applications in the development of pharmaceuticals. Its unique structure and reactivity make it a promising candidate for the synthesis of biologically active compounds with potential therapeutic properties.
Used in Bioconjugate Synthesis:
1,3,4-tri-O-acetyl-2-(acetylamino)-2-deoxy-6-O-tritylhexopyranose is also used in the synthesis of bioconjugates, which are hybrid molecules composed of biologically active components linked to other molecules. The trityl group at position 6 provides a convenient handle for attaching various functional groups, making it suitable for the development of bioconjugates with specific applications in research and therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 10026-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,2 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10026-54:
(7*1)+(6*0)+(5*0)+(4*2)+(3*6)+(2*5)+(1*4)=47
47 % 10 = 7
So 10026-54-7 is a valid CAS Registry Number.

10026-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 3-(acetylamino)-2,5-di(acetyloxy)-6-[(trityloxy)methyl]tetrahydro-2h-pyran-4-yl acetate

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:10026-54-7 SDS

10026-54-7Downstream Products

10026-54-7Relevant academic research and scientific papers

Non-mucin type synthetic compounds or its carrier conjugated compounds

-

, (2008/06/13)

The purposes of this invention are preparation of the non-mucin type synthetic compounds-carrier conjugated compounds which are stable against enzymes, and which have the ability of specific reactivity to induce immune response for cancer and HIV. A compo

FLUORINATED CARBOHYDRATES AS POTENTIAL PLASMA MEMBRANE MODIFIERS AND INHIBITORS. SYNTHESIS OF 2-ACETAMIDO-2,6-DIDEOXY-6-FLUORO-D-GALACTOSE

Sharma, Moheswar,Potti, Gopalan G.,Simmons, Onda D.,Korytnyk, Walter

, p. 41 - 52 (2007/10/02)

Reaction of benzyl 2-acetamido-3,4-di-O-benzyl-2-deoxy-6-O-mesyl-α-D-galactopyranoside with cesium fluoride gave benzyl 2-acetamido-3,6-anhydro-4-O-benzyl-2-deoxy-α-D-galactopyranoside instead of the desired 6-fluoro derivative.Acetonation of benzyl 2-ace

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