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425427-88-9

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425427-88-9 Usage

Description

6-CHLORO-3-INDOXYL-ALPHA-D-MANNOPYRANOSIDE is a synthetic compound that serves as a chromogenic substrate for the enzyme α-mannosidase. It is characterized by its ability to produce a salmon-colored precipitate upon enzymatic cleavage, which makes it a useful tool in various applications.

Uses

Used in Diagnostic Applications:
6-CHLORO-3-INDOXYL-ALPHA-D-MANNOPYRANOSIDE is used as a diagnostic agent for the detection and monitoring of α-mannosidase activity. The enzyme plays a crucial role in the metabolism of complex carbohydrates, and its abnormal activity can be indicative of certain health conditions. The salmon-colored precipitate produced upon cleavage allows for easy visualization and assessment of the enzyme's activity.
Used in Research and Development:
In the field of research and development, 6-CHLORO-3-INDOXYL-ALPHA-D-MANNOPYRANOSIDE is used as a research tool for studying the function and regulation of α-mannosidase. Its chromogenic properties make it an ideal candidate for investigating the enzyme's role in various biological processes and its potential as a therapeutic target for certain diseases.
Used in Pharmaceutical Industry:
6-CHLORO-3-INDOXYL-ALPHA-D-MANNOPYRANOSIDE is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs targeting α-mannosidase-related conditions.
Used in Quality Control:
In the quality control of pharmaceutical products, 6-CHLORO-3-INDOXYL-ALPHA-D-MANNOPYRANOSIDE can be used as a reference standard or control substance to ensure the accuracy and reliability of α-mannosidase activity assays. This helps in maintaining the quality and consistency of diagnostic tests and therapeutic products that rely on the measurement or modulation of α-mannosidase activity.

Check Digit Verification of cas no

The CAS Registry Mumber 425427-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,5,4,2 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 425427-88:
(8*4)+(7*2)+(6*5)+(5*4)+(4*2)+(3*7)+(2*8)+(1*8)=149
149 % 10 = 9
So 425427-88-9 is a valid CAS Registry Number.

425427-88-9SDS

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 (2R,3S,4S,5S,6R)-2-[(6-chloro-1H-indol-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names W0486

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:425427-88-9 SDS

425427-88-9Downstream Products

425427-88-9Relevant articles and documents

Substrate and preparation method and application thereof

-

Paragraph 0022; 0026, (2019/05/15)

The invention discloses a substrate namely alpha-D-glucoside for detecting activity of alpha-glucosidases, and further discloses a synthesis technology of the substrate. The synthesis technology comprises the steps of enabling a compound alpha-D-glucose and acetyl chloride to be subjected to a reaction, and performing purification to obtain alpha-D- pentacetylglucose; catalyzing the obtained substances with N,N-Dimethyl-1,3-diaminopropane, performing pickling, performing extraction, performing drying, and performing purifying to obtain 2,3,4,6-tetra-O-acetyl-alpha-D-acetyl-glucosamine; catalyzing the obtained substances in a dichloromethane solution, performing a reaction with trichloroacetonitrile, performing filtering, and performing purifying to obtain 2,3,4,6-tetra-O-acetyl-beta-D-glucosyl trichloroacetimidate; performing catalyzing on the obtained substances in a dichloromethane solution, performing a reaction with chromogen or fluorophore, performing extraction, merging organic phases, performing drying, performing concentrating, performing methanol redissolution, performing crystal nourishing at 4 DEG C, and performing filtering to obtain 2,3,4,6-tetra-O-acetyl-alpha-D-glucoside; and catalyzing the obtained substances in a methanolic solution, performing a reaction, then performing decoloring adsorption, performing filtering, and performing purifying. The synthesis technology of the substrate is simple and high in yield, the sensitivity of a reagent kit can be improved, the stability is good, and the specificity is high.

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