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14934-27-1

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14934-27-1 Usage

Description

(1Z)-1-[2-(4-hydroxyphenyl)hydrazinylidene]naphthalen-2(1H)-one is a hydrazine derivative featuring a naphthalene backbone and a hydroxyphenyl group. This chemical compound is widely utilized in organic synthesis and pharmaceutical research due to its unique molecular structure and functional groups, which make it a valuable building block for the development of novel pharmaceutical compounds and therapeutic agents.

Uses

Used in Pharmaceutical Research:
(1Z)-1-[2-(4-hydroxyphenyl)hydrazinylidene]naphthalen-2(1H)-one is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its molecular structure allows for the creation of new drugs and therapeutic agents, making it a promising candidate for medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, (1Z)-1-[2-(4-hydroxyphenyl)hydrazinylidene]naphthalen-2(1H)-one serves as a versatile building block. Its hydroxyphenyl group and naphthalene backbone enable the formation of a wide range of organic compounds, contributing to the advancement of chemical research and development.
Further research into the properties and potential uses of (1Z)-1-[2-(4-hydroxyphenyl)hydrazinylidene]naphthalen-2(1H)-one is ongoing, as its unique characteristics hold promise for future applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 14934-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,3 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14934-27:
(7*1)+(6*4)+(5*9)+(4*3)+(3*4)+(2*2)+(1*7)=111
111 % 10 = 1
So 14934-27-1 is a valid CAS Registry Number.

14934-27-1SDS

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 (1Z)-1-[(4-hydroxyphenyl)hydrazinylidene]naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 1-<2-Hydroxy-1-benzolazo>-4-hydroxy-naphthalin

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:14934-27-1 SDS

14934-27-1Relevant articles and documents

New generation of nitrite functionalized star-like polyvinyl imidazolium compound: Application as a nitrosonium source and three dimensional nanocatalyst for the synthesis of azo dyes

Shomali, Ashkan,Valizadeh, Hassan,Noorshargh, Saeideh

, p. 409 - 418 (2017/07/24)

The compounds with three-dimensional and ionic structures have attracted considerable attentions because of their unique characteristics as a drug carrier and catalyst. Star-like poly ionic compounds are a new generation of three-dimensional structures which have both; the exclusive ionic features and three-dimensional structures. Recently, we reported the synthesis of diazonium salts from aniline derivatives using carboxyl and nitrite functionalized graphene quantum dots. Methods: Nitrite-functionalized star-like polyionic (NFSP) compound was synthesized as a new generation of three-dimensional nanocatalyst. Herein, the use of NFSP as an efficient reagent and nanocatalyst for the diazotization of aniline derivatives and subsequent synthesis of azo dyes via the reaction with active phenolates under solvent-free conditions was reported. Results: In order to demonstrate the positive impact of NFSP efficiency, the reaction times and yields of the products were compared with other methods and catalysts which have been reported previously. The brilliant performance of NFSP can be ascribed to multifunctional reagent and also trapping the ingredient within catalyst cavities. Conclusion: A highly effective and cost-effective method has been developed for the preparation of azo dyes. In reported method, new three-dimensional catalyst with highly ionic characteristic and multifunctional nitrosonium source is available. These special features reduced the required amount of catalyst, reaction time and also increased the efficiency of catalyst.

Carboxyl and nitrite functionalized graphene quantum dots as a highly active reagent and catalyst for rapid diazotization reaction and synthesis of azo-dyes under solvent-free conditions

Valizadeh, Hassan,Shomali, Ashkan,Nourshargh, Saideh,Mohammad-Rezaei, Rahim

, p. 522 - 528 (2015/03/18)

Carboxyl and nitrite functionalized graphene quantum dots was prepared from carboxyl and hydroxyl functionalized graphene quantum dots using NaNO2 in the absence of mineral acids. This functional group conversion was confirmed by FT-IR spectroscopy, photoluminescence and X-ray diffraction. The carboxyl and nitrite functionalized graphene quantum dots was used as an effective nitrosonium ion source and reusable catalyst for the efficient diazotization of a variety of arylamines without using any additional acid. Subsequent azo-coupling of these freshly prepared diazonium salts with a range of active aromatic compounds led to the requisite azo-dyes in excellent yields in very short reaction times with a simple experimental procedure.

A new nitrite ionic liquid (IL-ONO) as a nitrosonium source for the efficient diazotization of aniline derivatives and in-situ synthesis of azo dyes

Valizadeh, Hassan,Shomali, Ashkan

experimental part, p. 1138 - 1143 (2012/03/27)

A new task-specific nitrite containing ionic liquid derived from the O-nitrosation of N-methyl-N-hydroxybutylimidazolinium chloride was synthesized and used as a source of nitrosonium ion to affect the efficient diazotization of arylamines. The diazonium salts thus obtained were coupled, using standard experimental procedures, to a range of tertiary anilines, phenols and naphthols to afford the requisite azo dyes in good yield. The diazotization and subsequent azo-coupling generated the related azo dyes at 0-5 °C in short reaction times with a simple experimental procedure.

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