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Acetamide, N-[2-[2-(2-aminoethoxy)ethoxy]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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866404-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866404-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,4,0 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 866404-69:
(8*8)+(7*6)+(6*6)+(5*4)+(4*0)+(3*4)+(2*6)+(1*9)=195
195 % 10 = 5
So 866404-69-5 is a valid CAS Registry Number.

866404-69-5SDS

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 Acetamide, N-[2-[2-(2-aminoethoxy)ethoxy]ethyl]-

1.2 Other means of identification

Product number -
Other names ACETAMIDE,N-[2-[2-(2-AMINOETHOXY)ETHOXY]ETHYL]-

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:866404-69-5 SDS

866404-69-5Downstream Products

866404-69-5Relevant academic research and scientific papers

Structural analysis of ATP analogues compatible with kinase-catalyzed labeling

Suwal, Sujit,Senevirathne, Chamara,Garre, Satish,Pflum, Mary Kay H.

, p. 2386 - 2391 (2013/02/23)

Kinase-catalyzed protein phosphorylation is an important biochemical process involved in cellular functions. We recently discovered that kinases promiscuously accept γ-modified ATP analogues as cosubstrates and used several ATP analogues as tools for stud

Phenyl esters, preferred reagents for mono-acylation of polyamines in the presence of water

Pappas, Kyrie,Zhang, Xiang,Tang, Wei,Fang, Shiyue

body text, p. 5741 - 5743 (2009/12/06)

In the presence of water, several diamines and one triamine were mono-acylated at ambient to moderate temperatures using phenyl esters and a phenyl carbonate as acylation agents in good to excellent isolated yields. Both linear and cyclic polyamines were suitable substrates, and the acylating agents can be aryl and alkyl carboxylic acid esters.

Mono-acylation of symmetric diamines in the presence of water

Tang, Wei,Fang, Shiyue

supporting information; scheme or table, p. 6003 - 6006 (2009/04/11)

Simply reacting equal equivalents of symmetric diamines with esters or carbonates in the presence of a suitable amount of water gave mono-acylated products in good to quantitative yields.

GELDANAMYCIN AND DERIVATIVES INHIBIT CANCER INVASION AND IDENTIFY NOVEL TARGETS

-

Page/Page column 37; 38, (2008/06/13)

Geldanamycin derivatives that block the uPA-plasmin network and inhibit growth and invasion by glioblastoma cells and other tumors at femtomolar concentrations are potentially highly active anti-cancer drugs. GA and various 17-amino-17-demethoxygelddanamycin derivatives are disclosed that block HGF/SF-mediated Met tyrosine kinase receptor-dependent uPA activation at fM levels. Other ansamycins (macbecins I and II), GA derivatives, and radicicol required concentrations several logs higher (≥nM) to achieve such inhibition. The inhibitory activity of tested compounds was discordant with the known ability of drugs of this class to bind to hsp90, indicating the existence of a novel target(s) for HGF/SF -mediated events in tumor development. Methods of using such compounds to inhibit cancer cell activities and to treat tumors are disclosed. Such treatment with low doses of these highly active compounds provide an option for treating various Met-expressing tumors, in particular invasive brain cancers, either alone or in combination with conventional surgery, chemotherapy, or radiotherapy.

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