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Ethanamine, 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-N-[2-[[(1,1-dimethylethyl)diphenyl silyl]oxy]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

189279-33-2

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189279-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189279-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,2,7 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 189279-33:
(8*1)+(7*8)+(6*9)+(5*2)+(4*7)+(3*9)+(2*3)+(1*3)=192
192 % 10 = 2
So 189279-33-2 is a valid CAS Registry Number.

189279-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name NH(CH2CH2OTBDPS)2

1.2 Other means of identification

Product number -
Other names N,N-[bis(2-tert-butyldiphenylsilyloxyethyl)]amine

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:189279-33-2 SDS

189279-33-2Relevant academic research and scientific papers

Design and assembly of new nonviral RNAi delivery agents by microwave-assisted quaternization (MAQ) of tertiary amines

Ghosh, Animesh,Mukherjee, Koushik,Jiang, Xinpeng,Zhou, Ying,McCarroll, Joshua,Qu, James,Swain, Pamela M.,Baigude, Huricha,Rana, Tariq M.

, p. 1581 - 1587 (2010)

RNA interference (RNAi) is a gene-silencing phenomenon whereby double-stranded RNA (dsRNA) triggers the sequence-specific degradation of homologous mRNA. RNAi has been quickly and widely applied to discover gene functions and holds great potential to prov

Aminolysis of cyclic thioxocarbonate of (R,R)-di-tert-butyl tartrate: Efficient access to thio- and thiolcarbamates

Faissat, Ludovic,Chavis, Claude,Montero, Jean-Louis,Lucas, Marc

, p. 1253 - 1259 (2002)

Aminolysis of cyclic thioxocarbonates derived from (R,R)-dialkyl tartrates with secondary amines is described to afford efficiently thio- and thiolcarbamates in a fast and high yielding reaction. Their stereochemistry and mechanism of formation are discus

CHEMICAL COMPOUNDS

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Page/Page column 40, (2012/02/15)

The present invention relates to compounds of Formula (I): and to their salts, pharmaceutical compositions, methods of use, and methods for their preparation. These compounds inhibit Bcl-2 and/or Bcl-XL activities and may be used for the treatment of cancer.

METHODS AND COMPOSITIONS FOR THE EFFICIENT DELIVERY OF THERAPEUTIC AGENTS TO CELLS AND ANIMALS

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Page/Page column 59-60; 6/17, (2008/06/13)

The present invention provides methods of carrying out the safe and reliable preparation of lipids comprising quaternary amines. Such lipids are especially suited for introducing therapeutic agents into cells or organisms. In particular, the lipids of the invention are suitable for the efficient transfer of gene therapy agents into mammalian cells or organisms in a cell type specific or tissue specific manner.

Formulations and methods for generating active cytofectin: polynucleotide transfection complexes

-

, (2008/06/13)

In the generation of cytofectin:polynucleotide complexes for transfection of cells, formulations, counterions, and reaction conditions for maximizing the transfection include using a cationic amine compound that has the general structure: STR1 wherein Rs

Polyfunctional cationic cytofectins, formulations and methods for generating active cytofectin: polynucleotide transfection complexes

-

, (2008/06/13)

Amine containing compounds and their use in the generation of cytofectin:polynucleotide complexes for transfection of cells, formulations, counterions, and reaction conditions for maximizing the transfection include using cationic amine compounds that hav

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