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Phenyl[2,3,4-tri-O-acetyl-6-O-(2,3,4,6-tetra-O-acetylhexopyranosyl)hexopyranosyl]oxyacetonitrile, also known as PTBN-CN, is a complex organic chemical compound with a molecular formula of C40H47NO17. It is a derivative of acetonitrile and features multiple acetyl and hexopyranosyl groups. PTBN-CN is recognized as an important synthetic intermediate in organic synthesis and pharmaceutical research, known for its potential role in the development of new drugs and pharmaceutical products. Its intricate molecular structure allows for modulation of biological activities in medicinal chemistry, highlighting its pharmacological significance.

5401-54-7

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5401-54-7 Usage

Uses

Used in Pharmaceutical Research:
PTBN-CN is utilized as a synthetic intermediate for the development of new drugs and pharmaceutical products. Its unique molecular structure enables the modulation of biological activities, making it a valuable compound in medicinal chemistry for creating innovative therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, PTBN-CN serves as a building block for the creation of complex organic molecules. Its versatile chemical properties allow for its incorporation into a wide range of synthetic pathways, contributing to the advancement of organic chemistry.
Used in Drug Development:
PTBN-CN is employed in drug development as a key component in the synthesis of potential pharmaceuticals. Its ability to modulate biological activities positions it as a promising candidate for the creation of novel therapeutic agents with specific pharmacological effects.
Used in Medicinal Chemistry:
In medicinal chemistry, PTBN-CN is used as a synthetic intermediate to explore and understand the structure-activity relationships of potential drug candidates. Its complex molecular structure provides a foundation for the design and optimization of new pharmaceuticals with improved efficacy and selectivity.
Overall, PTBN-CN is a versatile and significant compound in the fields of pharmaceutical research, organic synthesis, drug development, and medicinal chemistry, offering a wide range of applications and potential for the creation of innovative therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 5401-54-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5401-54:
(6*5)+(5*4)+(4*0)+(3*1)+(2*5)+(1*4)=67
67 % 10 = 7
So 5401-54-7 is a valid CAS Registry Number.

5401-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,4,5-triacetyloxy-6-[[3,4,5-triacetyloxy-6-[cyano(phenyl)methoxy]oxan-2-yl]methoxy]oxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names heptaacetylamygdalin

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:5401-54-7 SDS

5401-54-7Downstream Products

5401-54-7Relevant academic research and scientific papers

Amygdalin as building block in oligosaccharide synthesis

Bliard, Christophe,Massiot, Georges,Nazabadioko, Serge

, p. 5083 - 5084 (1993)

Acetobromogentiobiose is prepared in two steps from amygdalin. Like other bromosugars it reacts on triphenylmethyl amygdalin derivatives with silver cyanide to afford tri-and tetrasaccharides in high yields.

USE OF AMYGDALIN ANALOGUES FOR THE TREATMENT OF PSORIASIS

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Page/Page column 6, (2008/06/13)

The compounds of formula (I), wherein n is an integer from 0 to 4; R1 is a radical selected from the group consisting of H, CH3, CH2-CH3, C(CH3)3, COOH, CONH2 and C≡CH; R2, R3, R4 and R5 ar

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