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4-(4-N,N-DIETHYLAMINOPHENYLAZO)ANILINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34295-45-9

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34295-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34295-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,9 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34295-45:
(7*3)+(6*4)+(5*2)+(4*9)+(3*5)+(2*4)+(1*5)=119
119 % 10 = 9
So 34295-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H20N4/c1-3-20(4-2)16-11-9-15(10-12-16)19-18-14-7-5-13(17)6-8-14/h5-12H,3-4,17H2,1-2H3/b19-18+

34295-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-N,N-DIETHYLAMINOPHENYLAZO)ANILINE

1.2 Other means of identification

Product number -
Other names 4-diethylamino-4'-aminodiazobenzene

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:34295-45-9 SDS

34295-45-9Relevant 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.

Synthesis and application of 4-diethylaminodiazabenzene-4'-isothiocyanate for the derivatization and chromatographic separation of biogenic amines

Pyra, Edmund,Wawrzycki, Slawomir,Modzelewska-Banachiewicz, Bozena

, p. 173 - 177 (2007/10/03)

4-Diethylaminodiazabenzene-4'-isothiocyanate (DEABITC) was synthetized and applied for the preparation of thiocarbamoyl derivatives of the amines possesing the constant ethylamine fragment. The coloured derivatives were separated using TLC. The results of

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