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(1E)-1,3-bis(3-chlorophenyl)triaz-1-ene is a chemical compound with the molecular formula C18H10Cl2N2. It is a triazene derivative, which refers to a class of compounds containing a triazene moiety. This particular compound is characterized by two 3-chlorophenyl groups attached to a triazene backbone, resulting in a conjugated system of alternating single and double bonds. Due to its unique molecular structure, it may have potential applications in various fields such as medicine, agriculture, and materials science.

17596-04-2

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17596-04-2 Usage

Uses

Used in Pharmaceutical Industry:
(1E)-1,3-bis(3-chlorophenyl)triaz-1-ene is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique chemical and physical properties make it a promising candidate for the development of new therapeutic agents.
Used in Agricultural Industry:
(1E)-1,3-bis(3-chlorophenyl)triaz-1-ene is used as a chemical intermediate in the production of agrochemicals. Its potential applications in this field include the development of new pesticides or herbicides.
Used in Materials Science:
(1E)-1,3-bis(3-chlorophenyl)triaz-1-ene is used as a building block for the synthesis of new materials with unique properties. Its conjugated system of alternating single and double bonds may contribute to the development of advanced materials for various applications.
Further research and experimentation are needed to fully understand and harness the potential of (1E)-1,3-bis(3-chlorophenyl)triaz-1-ene in these and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 17596-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,9 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17596-04:
(7*1)+(6*7)+(5*5)+(4*9)+(3*6)+(2*0)+(1*4)=132
132 % 10 = 2
So 17596-04-2 is a valid CAS Registry Number.

17596-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis-(3-chloro-phenyl)-triazene

1.2 Other means of identification

Product number -
Other names m,m'-Dichlordiazoaminobenzol

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:17596-04-2 SDS

17596-04-2Relevant academic research and scientific papers

Pigment dispersion, method for manufacturing toner, aqueous ink, and triazo compound

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Page/Page column 32; 33, (2020/07/02)

A pigment dispersion has low viscosity and good dispersion property without depending on pigment species. The pigment dispersion contains a dispersion medium, an organic pigment, and a triazo compound having a specific structure.

Synthesis and properties of amphiphilic photoresponsive gelators for aromatic solvents

Rajaganesh, Ramanathan,Gopal, Anesh,Mohan Das, Thangamuthu,Ajayaghosh, Ayyappanpillai

supporting information; experimental part, p. 748 - 751 (2012/03/26)

A sugar-based photoresponsive supergelator, N-glycosylazobenzene that shows selective gelation of aromatic solvents is described. The partial trans - cis isomerization of the azobenzene moiety allows photoinduced chopping of the entangled gel fibers to short fibers, resulting in controlled fiber length and gel - sol transition. The gelator is useful for the selective removal of toxic aromatic solvents from water.

SUBSTITUENT EFFECT ON SOLVOLYSIS OF 3-ACETYL-1,3-DIPHENYLTRIAZENES

Pytela, Oldrich,Pilny, Miroslav,Vecera, Miroslav

, p. 1173 - 1181 (2007/10/02)

Eleven symmetrically disubstituted 3-acetyl-1,3-diphenyltriazenes have been synthetized by a new method.The solvolysis kinetics of title compounds has been measured in 20percent aqueous ethanol at several temperatures.The results are discussed from the point of view of temperature and substituent effects on the solvolysis rate constant of the 3-acetyl-1,3-diphenyltriazenes and conclusions are drawn about the reaction mechanism.

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