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97794-07-5

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  • (2Z)-2-[[2-CHLORO-4-[3-CHLORO-4-[(2Z)-2-[2-OXO-1-(PHENYLCARBAMOYL)PROPYLIDENE]HYDRAZINYL]PHENYL]PHENYL]HYDRAZINYLIDENE]-3-OXO-N-PHENYL-BUTANAMIDECAS

    Cas No: 97794-07-5

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97794-07-5 Usage

General Description

"(2Z)-2-[[2-chloro-4-[3-chloro-4-[(2Z)-2-[2-oxo-1-(phenylcarbamoyl)propylidene]hydrazinyl]phenyl]phenyl]hydrazinylidene]-3-oxo-N-phenyl-butanamide is a complex organic compound with a long chemical structure. It contains multiple chloro and phenyl groups, along with a carbamoyl and hydrazinyl functional groups. The compound is in the form of a butanamide, and it has two hydrazinylidene moieties. The presence of multiple functional groups and the long, complex structure indicate that this compound is likely to have various chemical and potentially biological activities."

Check Digit Verification of cas no

The CAS Registry Mumber 97794-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,9 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97794-07:
(7*9)+(6*7)+(5*7)+(4*9)+(3*4)+(2*0)+(1*7)=195
195 % 10 = 5
So 97794-07-5 is a valid CAS Registry Number.

97794-07-5SDS

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 2-[[4-[4-[2-(1-anilino-1,3-dioxobutan-2-ylidene)hydrazinyl]-3-chlorophenyl]-2-chlorophenyl]hydrazinylidene]-3-oxo-N-phenylbutanamide

1.2 Other means of identification

Product number -
Other names (2Z)-2-[[2-CHLORO-4-[3-CHLORO-4-[(2Z)-2-[2-OXO-1-(PHENYLCARBAMOYL)PROPYLIDENE]HYDRAZINYL]PHENYL]PHENYL]HYDRAZINYLIDENE]-3-OXO-N-PHENYL-BUTANAMIDE

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:97794-07-5 SDS

97794-07-5Downstream Products

97794-07-5Relevant articles and documents

A quantitative one-pot synthesis method for industrial azo pigments with recyclable wastewater

Feng, Guangyuan,Zhu, Meiling,Liu, Lei,Li, Chunbao

supporting information, p. 1769 - 1776 (2019/04/08)

Most industrial azo pigments are synthesized by diazotization in one pot and then coupling in another. This two-pot process has been transformed into a one-pot method by adding granular PTFE (polytetrafluoroethylene) to a mechanically agitated aqueous mixture of NaNO2, HCl, a diazo component and a coupling component. This method avoids the step of using a base or a surfactant to dissolve the coupling component. The reactions were fast and quantitative. The granular PTFE, wastewater and excess HCl were then reused 11 times without deteriorating the reaction rate and product purity. Altogether, 22 industrial pigments and 3 azo compounds were synthesized and the reaction can produce up to 22.7 g of product in the laboratory. Some reactions require less than 2 equiv. of HCl and a mechanism explaining this is proposed. In addition, an o-nitro group effect is advanced to explain the differences in coupling reaction rates for o-, m- and p-nitroaniline.

Production process and system for insoluble azo pigments

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Page/Page column 11-12, (2008/06/13)

An insoluble azo pigment is produced by ejecting a diazo solution and a grounding solution continuously into an ejector such that within the ejector, the diazo solution and grounding solution are mixed with each other and are subjected to a coupling reaction. A production system for the insoluble azo pigment includes the following units (1) to (4): (1) a first feed tank (2) for a first fluid selected from the diazo solution or grounding solution, a first flow path (a) for feeding the first fluid to nozzles of an ejector (1), and a pump (d) for feeding the first fluid through the first flow path; (2) the ejector (1) provided with the nozzles, a suction chamber, a diffuser, and a temperature control device (g); (3) a second feed tank (3) for a second fluid, a second flow path (b) for guiding the second fluid into the suction chamber, and a flow control device (e) for controlling a flow rate of the second fluid through the second flowpath (b); and (4) a heat treatment tank (5) for subjecting to heat treatment a suspension of the insoluble azo pigment formed by a reaction between the first fluid and the second fluid, and a third flow path (a′) for guiding the suspension from the diffuser to the heat treatment tank.

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