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2-imino-2-methoxyethyl-1-thio-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75204-21-6

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75204-21-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75204-21-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,0 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75204-21:
(7*7)+(6*5)+(5*2)+(4*0)+(3*4)+(2*2)+(1*1)=106
106 % 10 = 6
So 75204-21-6 is a valid CAS Registry Number.

75204-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-3-carbethoxy-4,5-dioxonaphthofuran

1.2 Other means of identification

Product number -
Other names 4,5-Dioxo-3-carbethoxy-2-phenyl-naphtho[1'.2':2.3]furan

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:75204-21-6 SDS

75204-21-6Downstream Products

75204-21-6Relevant academic research and scientific papers

AGENTS FOR CLEARING BIOMOLECULES FROM CIRCULATION

-

Paragraph 0148, (2013/10/22)

Described is a method, and a combination of agents for used therein, by which an agent administered to a subject can be rapidly cleared from circulation. This is achieved by providing an Administration Agent (e.g. a probe for pretargeting) with a reactive group and providing a Clearing Agent with another reactive group, said reactive groups forming a bio-orthogonally reactive pair. Preferably, the reactive pair comprises a cyclooctene or cyclooctyn as one reactant, and a diene as the other reactant. The method and combination can be used for the removal of any bindable molecule from circulation, such as an excess of a pre-targeting probe in the course of a pre-targeting method, a targeting or imaging agent delivered, or the removal of any biomolecule already present in circulation.

Glycoviruses: Chemical glycosylation retargets adenoviral gene transfer

Pearce, Oliver M. T.,Fisher, Kerry D.,Humphries, Julia,Seymour, Leonard W.,Smith, Alberto,Davis, Benjamin G.

, p. 1057 - 1061 (2007/10/03)

A sugar-specific transfection mechanism is introduced by the glycosylation of adenoviruses (AVs, see picture), and manipulation of the glycosylation pattern allows the selective transfection of human macrophages in favor of the usual target. This dramatic retargeting holds promise for the fine-tuning of adenoviruses for applications such as gene therapy.

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