114747-45-4 Usage
Description
Technocolor Purple 3, also known as 1,3,3-Trimethyl-6''-(piperidin-1-yl)spiro[indoline-2,3''-naphtho[2,1-b][1,4]oxazine], is a synthetic compound with unique optical properties. It is characterized by its ability to modulate fluorescence in response to light, making it a promising candidate for various applications in different industries.
Uses
Used in Optical Applications:
Technocolor Purple 3 is used as a light-controlled fluorescent modulating material for its ability to alter its fluorescence properties under different light conditions. This characteristic makes it suitable for applications where precise control of light emission is required.
Used in Research and Development:
In the field of scientific research, Technocolor Purple 3 serves as a valuable tool for studying the behavior of light-sensitive materials and their potential applications in various fields, such as optoelectronics and photonics.
Used in Pharmaceutical Industry:
Technocolor Purple 3 can be utilized in the development of light-activated drugs, where the compound's fluorescence properties can be harnessed to track drug delivery and release in the body, providing valuable insights into drug efficacy and distribution.
Used in Security Features:
Due to its unique optical properties, Technocolor Purple 3 can be employed in the creation of security features for documents, currency, and other items that require authentication. Its light-sensitive nature can be used to create features that are difficult to forge or replicate.
Used in Display Technology:
In the display industry, Technocolor Purple 3 can be used to develop advanced display technologies that offer improved color accuracy, contrast, and energy efficiency by leveraging the compound's ability to modulate fluorescence in response to light.
Check Digit Verification of cas no
The CAS Registry Mumber 114747-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,4 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114747-45:
(8*1)+(7*1)+(6*4)+(5*7)+(4*4)+(3*7)+(2*4)+(1*5)=124
124 % 10 = 4
So 114747-45-4 is a valid CAS Registry Number.
114747-45-4Relevant articles and documents
Photochromism and solvatochromism of push-pull or pull-push spiroindolinenaphthoxazines
Metelitsa,Lokshin,Micheau,Samat,Guglielmetti,Minkin
, p. 4340 - 4345 (2002)
The photochromic and solvatochromic behaviour of 17 variously substituted spiroindoline naphthoxazines has been investigated in cyclohexane, toluene, acetonitrile and methanol in fluid solution. Specific parameters such as the wavelengths and the molar ab
One-pot synthesis of photochromic 6′-amino-substituted spirooxazines from 1-nitroso-2-naphthol zinc chelate and indoline base
Pang, Mei-Li,Zhang, Hui-Juan,Liu, Pei-Pei,Zou, Zhi-Hong,Han, Jie,Meng, Ji-Ben
experimental part, p. 3418 - 3422 (2010/11/20)
A series of spirooxazine derivatives containing nitrogen heterocycles were synthesized through the condensation of 2-methylene-1,3,3-trimethylindoline derivatives with the zinc salt of 1-nitroso-2-naphthol using ethanol as solvent. The method is simple, starts from readily accessible and inexpensive reagents, and leads to the synthesis of 6′-substituted spirooxazines in moderate to good yields. We simplified the workup and found that, for some target compounds, recrystallization can effectively improve efficiency of the separation and purification. Georg Thieme Verlag Stuttgart.
One-pot synthesis of 6′-amino-substituted spirooxazines
Koshkin,Lokshin,Samat,Gromov,Fedorova
, p. 1876 - 1880 (2007/10/03)
A one-pot synthesis of 6′-amino-substituted spiroindolinonaphth[2,1- b][1,4]oxazines is developed through the condensation of 2-methylene-1,3,3- trimethylindoline derivatives and 1-amino-2-naphthol in the presence of different secondary amines and oxidizing agents using methanol or toluene as the solvent. The main advantage of the method is its simplicity, and starting from readily accessible reagents, it allows the preparation of amino derivatives of spironaphthoxazine with good yields under mild reaction conditions. Georg Thieme Verlag Stuttgart.