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735-40-0

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735-40-0 Usage

General Description

Ethyl {[2-nitro-4-(trifluoromethyl)phenyl]amino}acetate is a chemical compound that belongs to the nitroaromatic and trifluoromethyl-substituted organic compounds. It is an ester derivative of the amino acid phenylalanine, with a nitro group and a trifluoromethyl group attached to the phenyl ring. This chemical is commonly used in organic synthesis and pharmaceutical research as a building block for the development of new drugs and agrochemicals. It exhibits potential biological activity and has been studied for its anti-inflammatory and anti-cancer properties. Ethyl {[2-nitro-4-(trifluoromethyl)phenyl]amino}acetate is a versatile compound with a wide range of applications in the field of chemistry and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 735-40-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 735-40:
(5*7)+(4*3)+(3*5)+(2*4)+(1*0)=70
70 % 10 = 0
So 735-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H11F3N2O4/c1-2-20-10(17)6-15-8-4-3-7(11(12,13)14)5-9(8)16(18)19/h3-5,15H,2,6H2,1H3

735-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[2-nitro-4-(trifluoromethyl)anilino]acetate

1.2 Other means of identification

Product number -
Other names 2-Nitro-4-trifluormethyl-phenylglycin-aethylester

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:735-40-0 SDS

735-40-0Relevant articles and documents

Chemical Targeting of Voltage Sensitive Dyes to Specific Cells and Molecules in the Brain

Fiala, Tomas,Wang, Jihang,Dunn, Matthew,?ebej, Peter,Choi, Se Joon,Nwadibia, Ekeoma C.,Fialova, Eva,Martinez, Diana M.,Cheetham, Claire E.,Fogle, Keri J.,Palladino, Michael J.,Freyberg, Zachary,Sulzer, David,Sames, Dalibor

supporting information, p. 9285 - 9301 (2020/06/04)

Voltage sensitive fluorescent dyes (VSDs) are important tools for probing signal transduction in neurons and other excitable cells. The impact of these highly lipophilic sensors has, however, been limited due to the lack of cell-specific targeting methods in brain tissue or living animals. We address this key challenge by introducing a nongenetic molecular platform for cell- and molecule-specific targeting of synthetic VSDs in the brain. We employ a dextran polymer particle to overcome the inherent lipophilicity of VSDs by dynamic encapsulation and high-affinity ligands to target the construct to specific neuronal cells utilizing only native components of the neurotransmission machinery at physiological expression levels. Dichloropane, a monoamine transporter ligand, enables targeting of dense dopaminergic axons in the mouse striatum and sparse noradrenergic axons in the mouse cortex in acute brain slices. PFQX in conjunction with ligand-directed acyl imidazole chemistry enables covalent labeling of AMPA-type glutamate receptors in the same brain regions. Probe variants bearing either a classical electrochromic ANEP dye or state-of-the-art VoltageFluor-type dye respond to membrane potential changes in a similar manner to the parent dyes, as shown by whole-cell patch recording. We demonstrate the feasibility of optical voltage recording with our probes in brain tissue with one-photon and two-photon fluorescence microscopy and define the signal limits of optical voltage imaging with synthetic sensors under a low photon budget determined by the native expression levels of the target proteins. This work demonstrates the feasibility of a chemical targeting approach and expands the possibilities of cell-specific imaging and pharmacology.

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