4485-89-6 Usage
Uses
Used in Chemical Synthesis:
3-Anilinoacrolein Anil is used as a reagent in the synthesis of various organic compounds, contributing to the formation of complex molecules and structures that are essential in different chemical processes.
Used in Dye Production:
In the dye industry, 3-Anilinoacrolein Anil is used as an intermediate, playing a crucial role in the production of dyes that impart color to various materials, including textiles, plastics, and paper.
Used in Pharmaceutical Manufacturing:
3-Anilinoacrolein Anil is employed as an intermediate in the manufacturing of pharmaceuticals, aiding in the development of new drugs and medicines that address a range of health conditions.
Used in Specialty Chemicals Production:
3-ANILINOACROLEIN ANIL is also utilized in the production of specialty chemicals, which are tailored for specific applications in industries such as agriculture, cosmetics, and coatings.
It is important to handle 3-Anilinoacrolein Anil with care and follow safety protocols to avoid exposure and adverse health effects, given its classification as a hazardous material.
Check Digit Verification of cas no
The CAS Registry Mumber 4485-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,8 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4485-89:
(6*4)+(5*4)+(4*8)+(3*5)+(2*8)+(1*9)=116
116 % 10 = 6
So 4485-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H14N2/c1-3-8-14(9-4-1)16-12-7-13-17-15-10-5-2-6-11-15/h1-13,16H/b12-7+,17-13+
4485-89-6Relevant academic research and scientific papers
Semisynthetic fluorescent sensor proteins based on self-labeling proteintags
Brun, Matthias A.,Tan, Kui-Thong,Nakata, Eiji,Hinner, Marlon J.,Johnsson, Kai
supporting information; experimental part, p. 5873 - 5884 (2009/09/24)
Genetically encoded fluorescent sensor proteins offer the possibility toprobe the concentration of key metabolites in living cells. The approac hes currently used to generate such fluorescent sensor proteins lack generality, as they require a protein that
Thermolysis of Polyazapentadienes. Part 6. Gas-phase Cyclisation of 1,5-Diaryl-1,5-diazapentadienes: Mechanistic Aspects and some Synthetic Applications
McNab, Hamish,Murray, M. Elizabeth-Ann
, p. 1565 - 1568 (2007/10/02)
The mode of formation of quinolines by gas-phase pyrolysis of 1,5-diaryl-1,5-diazapentadienes is contrasted with the thermal behaviour of 1,2,5-triazapentadienes.The mechanism involves concerted ring closure followed by a rapid 1,5-hydrogen shift to give a 3,4-dihydroquinoline intermediate, e.g. (19) or (21).Subsequent aromatisation takes place by a stepwise, free-radical process.Methylquinolines (9), (10), (12), and (13) were obtained on a preparative scale by this method.
