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N-ethyl-N-[p-[(p-nitrophenyl)azo]phenyl]benzylamine is a complex organic compound with the chemical formula C20H20N4O2. It is characterized by a benzylamine core, which is an aromatic amine with a benzyl group attached to the nitrogen atom. The molecule features a p-nitrophenylazo group, which is a chromophore responsible for its color, attached to a phenyl ring. This structure is further connected to an ethyl group, enhancing the solubility and reactivity of the compound. It is often used as a dye or pigment in various industrial applications due to its ability to absorb and reflect light, giving it a distinct color. The compound's specific structure and properties make it a valuable component in the field of color chemistry, particularly in the production of colored materials for textiles, plastics, and other industries.

3025-78-3

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3025-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3025-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3025-78:
(6*3)+(5*0)+(4*2)+(3*5)+(2*7)+(1*8)=63
63 % 10 = 3
So 3025-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H20N4O2/c1-2-24(16-17-6-4-3-5-7-17)20-12-8-18(9-13-20)22-23-19-10-14-21(15-11-19)25(26)27/h3-15H,2,16H2,1H3/b23-22+

3025-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-N-ethyl-4-[(4-nitrophenyl)diazenyl]aniline

1.2 Other means of identification

Product number -
Other names EINECS 221-183-5

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:3025-78-3 SDS

3025-78-3Downstream Products

3025-78-3Relevant academic research and scientific papers

Tuning photochromic ion channel blockers

Mourot, Alexandre,Kienzler, Michael A.,Banghart, Matthew R.,Fehrentz, Timm,Huber, Florian M. E.,Stein, Marco,Kramer, Richard H.,Trauner, Dirk

, p. 536 - 543 (2015/02/02)

Photochromic channel blockers provide a conceptually simple and convenient way to modulate neuronal activity with light. We have recently described a family of azobenzenes that function as tonic blockers of Kv channels but require UV-A light to unblock and need to be actively switched by toggling between two different wavelengths. We now introduce red-shifted compounds that fully operate in the visible region of the spectrum and quickly turn themselves off in the dark. Furthermore, we have developed a version that does not block effectively in the dark-adapted state, can be switched to a blocking state with blue light, and reverts to the inactive state automatically. Photochromic blockers of this type could be useful for the photopharmacological control of neuronal activity under mild conditions.

Novel azo disperse dyes derived from N-benzyl-N-ethyl-aniline: Synthesis, solvatochromic and optical properties

Yazdanbakhsh,Mohammadi,Mohajerani,Nemati,Nataj, N. Hosain,Moheghi,Naeemikhah

experimental part, p. 107 - 112 (2010/11/05)

Seven new azo disperse dyes based on N-benzyl-N-ethyl-aniline were synthesized and characterized by UV-Vis, FT-IR and 1H NMR spectroscopic techniques. The UV-visible studies and solvatochromic behavior of all dyes in 15 solvents with different polarity were examined and a meaningful correlation was observed. In the optical characterization of dyes using Z-Scan experiment, thin films of polymethyl metacrylate doped with guest synthesized chromophores 2, 3, 4 and 7 were investigated.

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