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trans-4-(4-(Aminomethyl)phenylazo)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

259199-82-1

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259199-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 259199-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,1,9 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 259199-82:
(8*2)+(7*5)+(6*9)+(5*1)+(4*9)+(3*9)+(2*8)+(1*2)=191
191 % 10 = 1
So 259199-82-1 is a valid CAS Registry Number.

259199-82-1Relevant academic research and scientific papers

Molecular design of photoswitchable surfaces with controllable wettability

Demirel, Goeken Birlik,Dilsiz, Nursel,Akmak, Mehmet,Aykara, Tuncer

experimental part, p. 3189 - 3196 (2011/10/08)

In this work, we developed a photocontrollable substrate which was prepared using an azobenzene-containing self-assembled monolayer (SAM) on the silicon surface via the chemisorption of 3-glycidoxypropyltrimethoxysilane (GPTS) and 4-(4′-aminophenylazo) benzoic acid (APABA). The prepared surfaces were chemically characterized by X-ray photoelectron spectroscopy (XPS). The reversible photoswitching performance of APABA molecules were investigated by UV spectroscopy in dimethylsulfoxide (DMSO) solution. To understand and control this reversible photoswitchable mechanism and wettability properties, contact angle measurements were performed by using a variety of liquids after UV and visible light irradiation. These contact angle results are used to approximate the components of the APABA-modified surface energy under UV and visible light using the Lifshitz-van der Waals/acid-base approach. The total surface energy (γs) after visible light irradiation (for trans formation) was calculated to be 37.28 mJ m-2, whereas the value after UV light exposure (for cis formation) was also calculated to be 36.95 mJ m-2. All the results demonstrate the great potential to control molecular events within and on the surfaces of molecular constructs using light. The Royal Society of Chemistry 2011.

Chromium complex compound

-

, (2008/06/13)

A chromium complex compound represented as the free acid form by the formula (I): STR1 wherein X1 represents a hydrogen atom, a methyl group, a methoxy group or a sulfonic acid group; X2, X3 and X4 represent independently a hydrogen atom, a chlorine atom, a methyl gorup, a methoxy group, a carboxyl group or a sulfonic acid group; Y represents a hydrogen atom or a sulfonic acid group; Z represents a chlorine atom, a fluorine atom or --N30 (R)3 (R represents a C1 to C4 -alkyl group), STR2 and M represents a hydrogen atom or an alkali metal, a process for producing the chromium complex compound (I) and a method for dyeing cellulosic fibers with the same. The chromium complex compound represented by formula (I) is excellent in affinity to cellulosic fibers and in color-yield, build-up properties and fastness properties. These compounds are dyes for cellulosic fibers.

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