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155172-86-4

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155172-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155172-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,1,7 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155172-86:
(8*1)+(7*5)+(6*5)+(5*1)+(4*7)+(3*2)+(2*8)+(1*6)=134
134 % 10 = 4
So 155172-86-4 is a valid CAS Registry Number.

155172-86-4SDS

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 3-[4-(dibutylamino)phenyl]-4-chlorocyclobut-3-ene-1,2-dione

1.2 Other means of identification

Product number -
Other names 4-(N,N-Dibutylaminophenyl)-3-chlorocyclobut-3-ene-1,2-dione

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:155172-86-4 SDS

155172-86-4Relevant articles and documents

Synthesis of novel unsymmetrical squarylium dyes absorbing in the near-infrared region

Yagi, Shigeyuki,Hyodo, Yutaka,Matsumoto, Shinya,Takahashi, Naoki,Kono, Hiroshi,Nakazumi, Hiroyuki

, p. 599 - 603 (2000)

Novel unsymmetrical squarylium dyes which absorb in the near-infrared region were synthesized by a stepwise procedure via intermediate 4-substituted 3-hydroxycyclobut-3-ene-1,2-diones. By introducing benz[c,d]indoline or benzo[b]pyran moieties at one end

Aggregation of a Surfactant Squaraine in Langmuir-Blodgett Films, Solids, and Solution

Chen, Huijuan,Herkstroeter, William G.,Perlstein, Jerome,Law, Kock-Yee,Whitten, David G

, p. 5138 - 5146 (1994)

The aggregation of a surfactant squaraine, 4-(N-methyl-N-(carboxypropyl)amino)phenyl-4'-(N,N-dibutylamino)phenylsquaraine (SBA), has been studied in a variety of media, including organic solvents, aqueous cyclodextrin (CD) solutions, vesicles, monolayers,

Asymmetrical squaraine cyanine dye probe based on substituted aniline, preparation method and application thereof

-

Paragraph 0025; 0027; 0030; 0032, (2018/04/02)

The invention belongs to the field of chemical analysis test and specifically relates to an asymmetrical squaraine cyanine dye probe based on substituted aniline as well as a preparation method and an application thereof. The method comprises the followin

Self-assembled near-infrared dye nanoparticles as a selective protein sensor by activation of a dormant fluorophore

Anees, Palapuravan,Sreejith, Sivaramapanicker,Ajayaghosh, Ayyappanpillai

supporting information, p. 13233 - 13239 (2015/03/30)

Design of selective sensors for a specific analyte in blood serum, which contains a large number of proteins, small molecules, and ions, is important in clinical diagnostics. While metal and polymeric nanoparticle conjugates have been used as sensors, small molecular assemblies have rarely been exploited for the selective sensing of a protein in blood serum. Herein we demonstrate how a nonspecific small molecular fluorescent dye can be empowered to form a selective protein sensor as illustrated with a thiol-sensitive near-IR squaraine ( Sq) dye (λabs= 670 nm, λem= 700 nm). The dye self-assembles to form non fluorescent nanoparticles (Dh = 200 nm) which selectively respond to human serum albumin (HSA) in the presence of other thiol-containing molecules and proteins by triggering a green fluorescence. This selective response of the dye nanoparticles allowed detection and quantification of HSA in blood serum with a sensitivity limit of 3 nM. Notably, the Sq dye in solution state is nonselective and responds to any thiol-containing proteins and small molecules. The sensing mechanism involves HSA specifi c controlled disassembly of the Sq nanoparticles to the molecular dye by a noncovalent binding process and its subsequent reaction with the thiol moiety of the protein, triggering the green emission of a dormant fluorophore present in the dye. This study demonstrates the power of a self-assembled small molecular fluorophore for protein sensing and is a simple chemical tool for the clinical diagnosis of blood serum.

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