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3H-Diazirine, 3-[4-(iodomethyl)phenyl]-3-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95758-92-2

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95758-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95758-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,5 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95758-92:
(7*9)+(6*5)+(5*7)+(4*5)+(3*8)+(2*9)+(1*2)=192
192 % 10 = 2
So 95758-92-2 is a valid CAS Registry Number.

95758-92-2Relevant academic research and scientific papers

NOVEL N-BENZYLAMIDE SUBSTITUTED DERIVATIVES OF 2-(ACYLAMIDO)ACETIC ACID AND 2-(ACYLAMIDO)PROPIONIC ACIDS: POTENT NEUROLOGICAL AGENTS

-

, (2009/12/27)

A first aspect of the invention is a compound (sometimes also referred to herein as an "active agent" or "active compound") of Formula (I) or ( Ia): or a pharmaceutically acceptable salt or prodrug thereof. Compositions thereof and methods of using the same (e.g. for the treatment of a neurological disease) are also described.

Trifluoromethyldiazirine: An effective photo-induced cross-linking probe for exploring amyloid formation

Smith, David P.,Anderson, Jon,Plante, Jeffrey,Ashcroft, Alison E.,Radford, Sheena E.,Wilson, Andrew J.,Parker, Martin J.

supporting information; experimental part, p. 5728 - 5730 (2009/04/13)

The separative and analytical power of ion mobility spectrometry-mass spectrometry combined with photo-induced cross-linking of site-specifically incorporated trifluoromethyldiazirine provides a powerful approach towards structural characterisation of amy

An efficient route to S-N-(9-fluorenylmethoxycarbonyl)-4′-(1-azi-2,2,2-trifluoroethyl) phenylalanine

Fishwick, Colin W. G.,Sanderson, John M.,Findlay, John B. C.

, p. 4611 - 4614 (2007/10/02)

An extremely efficient synthesis of optically pure photoactivatable phenylalanine derivative 1 is described. The key step involves a highly diastereoselective alkylation of a chiral glycine equivalent.

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