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Acetamide, N-[3,5-bis(trifluoromethyl)phenyl]-2-cyano- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63035-03-0

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63035-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63035-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,3 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63035-03:
(7*6)+(6*3)+(5*0)+(4*3)+(3*5)+(2*0)+(1*3)=90
90 % 10 = 0
So 63035-03-0 is a valid CAS Registry Number.

63035-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[3,5-bis(trifluoromethyl)phenyl]-2-cyanoacetamide

1.2 Other means of identification

Product number -
Other names N1-[3,5-di(trifluoromethyl)phenyl]-2-cyanoacetamide

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:63035-03-0 SDS

63035-03-0Relevant academic research and scientific papers

Synthesis characterization and biological evaluation of some novel amino pyrazole derivatives

Shah, Nilay,Patel, Pineshkumar N.,Karia, Denish C.

, p. 2647 - 2651 (2018)

Amino pyrazole and their derivatives for their biological activities. Present work describes the synthesis of novel amino pyrazole derivatives and evaluation of their medicinal value. The reaction of 3,5-bis(trifluoromethyl) aniline with cyano acetic acid

Agonist-mediated switching of ion selectivity in TPC2 differentially promotes lysosomal function

Gerndt, Susanne,Chen, Cheng-Chang,Chao, Yu-Kai,Yuan, Yu,Burgstaller, Sandra,Rosato, Anna Scotto,Krogsaeter, Einar,Urban, Nicole,Jacob, Katharina,Nguyen, Ong Nam Phuong,Miller, Meghan T.,Keller, Marco,Vollmar, Angelika M.,Gudermann, Thomas,Zierler, Susanna,Schredelseker, Johann,Schaefer, Michael,Biel, Martin,Malli, Roland,Wahl-Schott, Christian,Bracher, Franz,Patel, Sandip,Grimm, Christian

, (2020/05/08)

Ion selectivity is a defining feature of a given ion channel and is considered immutable. Here we show that ion selectivity of the lysosomal ion channel TPC2, which is hotly debated (Calcraft et al., 2009; Guo et al., 2017; Jha et al., 2014; Ruas et al., 2015; Wang et al., 2012), depends on the activating ligand. A high-throughput screen identified two structurally distinct TPC2 agonists. One of these evoked robust Ca2+-signals and non-selective cation currents, the other weaker Ca2+-signals and Na+-selective currents. These properties were mirrored by the Ca2+- mobilizing messenger, NAADP and the phosphoinositide, PI(3,5)P2, respectively. Agonist action was differentially inhibited by mutation of a single TPC2 residue and coupled to opposing changes in lysosomal pH and exocytosis. Our findings resolve conflicting reports on the permeability and gating properties of TPC2 and they establish a new paradigm whereby a single ion channel mediates distinct, functionally-relevant ionic signatures on demand.

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