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tert-butyl 2-(5-bromo-2-nitrophenyl)ethanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

878672-60-7

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878672-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 878672-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,6,7 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 878672-60:
(8*8)+(7*7)+(6*8)+(5*6)+(4*7)+(3*2)+(2*6)+(1*0)=237
237 % 10 = 7
So 878672-60-7 is a valid CAS Registry Number.

878672-60-7Relevant academic research and scientific papers

Light-induced protein dimerization by one- And two-photon activation of gibberellic acid derivatives in living cells

Schelkle, Korwin M.,Griesbaum, Tristan,Ollech, Dirk,Becht, Steffy,Buckup, Tiago,Hamburger, Manuel,Wombacher, Richard

supporting information, p. 2825 - 2829 (2015/03/04)

We developed a highly efficient system for light-induced protein dimerization in live cells using photo-caged derivatives of the phytohormone gibberellic acid (GA3). We demonstrate the application of the photo-activatable chemical inducer of di

Water-soluble, donor-acceptor biphenyl derivatives in the 2-(o-nitrophenyl)propyl series: Highly efficient two-photon uncaging of the neurotransmitter γ-aminobutyric acid at λ=800 nm

Donato, Loic,Mourot, Alexandre,Davenport, Christopher M.,Herbivo, Cyril,Warther, David,Leonard, Jeremie,Bolze, Frederic,Nicoud, Jean-Francois,Kramer, Richard H.,Goeldner, Maurice,Specht, Alexandre

supporting information; experimental part, p. 1840 - 1843 (2012/04/04)

Rattling the cage: The two γ-aminobutyric acid (GABA) derivatives 1 and 2 exhibit efficient and rapid (-6 s) GABA photorelease upon one-photon excitation combined with two-photon uncaging cross-section at λ=800 nm. Compounds 1 and 2 were

COMPOUNDS FOR TREATING NEURODEGENERATIVE DISEASES

-

Page/Page column 76, (2011/11/01)

The invention provides novel tricyclic compounds of Formula (I) that inhibit B-secretase cleavage of APP and are useful as therapeutic agents for treating neurodegenerative diseases.

Palladium-catalyzed synthesis of 3-indolecarboxylic acid derivatives

Soederberg, Bjoern C. G.,Banini, Serge R.,Turner, Michael R.,Minter, Aaron R.,Arrington, Amanda K.

, p. 903 - 912 (2008/09/21)

Indoles having an ester functionality in the 3-position were prepared from 2-(2-nitrophenyl)propenoic acid derivatives via a palladium-catalyzed reductive N-heteroannulation using carbon monoxide as the ultimate reducing agent. The starting materials were

DEVELOPMENT OF FLUOROGENIC SUBSTRATES FOR MONOAMINE OXIDASES (MAO-A AND MAO-B)

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Page/Page column 88; 129-130, (2008/06/13)

The present invention relates to compounds useful for detecting the activity of monoamine oxidases, compounds useful for competitively inhibiting monoamine oxidases, for determining inhibitors of monoamine oxidases and compounds useful for treating monoamine oxidase-related nervous system pathologies, as well as pharmaceutical compositions and methods of manufacture thereof.

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