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4-[2-(2-Fluorophenyl)vinyl]-N,N-dimethylaniline is an organic compound with the molecular formula C15H14FN. It is a derivative of aniline, featuring a 2-fluorophenyl group attached to a vinyl group, which in turn is connected to a 4-dimethylaminophenyl moiety. 4-[2-(2-Fluorophenyl)vinyl]-N,N-dimethylaniline is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used in the synthesis of various dyes, pigments, and pharmaceuticals due to its unique chemical structure and properties. The presence of the fluorine atom in the molecule can influence its reactivity and stability, making it a valuable intermediate in the chemical industry.

959-73-9

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959-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 959-73-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 959-73:
(5*9)+(4*5)+(3*9)+(2*7)+(1*3)=109
109 % 10 = 9
So 959-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H16FN/c1-18(2)15-11-8-13(9-12-15)7-10-14-5-3-4-6-16(14)17/h3-12H,1-2H3

959-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(2-Fluorophenyl)vinyl]-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names trans-dec-4-enoic acid

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:959-73-9 SDS

959-73-9Relevant academic research and scientific papers

Transition-metal-free method for the synthesis of benzo[b]thiophenes from o -halovinylbenzenes and K2S via direct SNAr-type reaction, cyclization, and dehydrogenation process

Zhang, Xiaoyun,Zeng, Weilan,Yang, Yuan,Huang, Hui,Liang, Yun

supporting information, p. 1687 - 1692 (2013/09/02)

A new, highly efficient procedure for the synthesis of benzothiophenes from easily available o-halovinylbenzenes and potassium sulfide has been developed. The reaction tolerated a wide range of functionalities, and various 2-substituted benzo[b]thiophenes

STILBENE ANALOGS AND METHODS OF TREATING CANCER

-

Page/Page column 15, (2012/08/08)

Stilbene analogs and pharmaceutical compositions that are useful for the treatment of various cancers, including without limitation, colorectal cancer (CRC) and breast cancer are disclosed. The halogenated stilbene analogs include nitrogen heteroaryl groups and/or amino groups on the stilbene ring.

Synthesis and evaluation of stilbene derivatives as a potential imaging agent of amyloid plaques

Hong, Myeng Chan,Kim, Yun Kyung,Choi, Jae Yong,Yang, Si Qiang,Rhee, Hakjune,Ryu, Young Hoon,Choi, Tae Hyun,Cheon, Gi Jeong,An, Gwang Il,Kim, Hye Yun,Kim, Youngsoo,Kim, Dong Jin,Lee, Jun-Seok,Chang, Young-Tae,Lee, Kyo Chul

experimental part, p. 7724 - 7730 (2011/01/13)

Fluorescence probes that can detect Aβ (β-amyloid peptide) plaque are important tools for diagnosis of Alzheimer's disease (AD), and 4-N-methylamino-4′-hydroxystilbene (SB-13) is one of the promising candidate molecules. We report here the synthesis of SB-13 derivatives that consist of various electron donating/withdrawing moieties and distinct size of N-substituents. The synthesized compounds were screened for detection of Aβ40 fibrils in vitro. Four compounds exhibited more than sixfold intensity increase, and they were further analyzed for detail bindings and Aβ plaque imaging. Among these molecules, compound 42 meets two critical requirements for imaging agent; high fluorescence responsiveness and strong binding affinity. This compound showed more than 25-fold increase with the dissociation constant of 1.13 ± 0.37 μM. In AD mouse brain tissue, 42 selectively stained Aβ plaque, more specifically peripheral regions of Aβ plaque. This finding demonstrated its potential use as brain-imaging agents for AD studies.

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