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96859-34-6

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96859-34-6 Usage

Description

5-(3-HYDROXYPHENYL) TETRAZOLE, also known as 3-(1H-Tetrazol-5-yl)phenol, is an organic compound with a unique structure that features a tetrazolyl group attached to a hydroxyphenyl moiety. 5-(3-HYDROXYPHENYL) TETRAZOLE exhibits interesting chemical and biological properties, making it a valuable building block in the synthesis of various pharmaceuticals and other organic compounds.

Uses

Used in Pharmaceutical Industry:
5-(3-HYDROXYPHENYL) TETRAZOLE is used as a key intermediate in the synthesis of Tetrazolylmethylamino Furazan-3-carboxylic Acid derivatives, which are compounds with potential anticancer properties. These derivatives are being investigated for their ability to target and treat various types of cancer, offering new therapeutic options for patients.

Check Digit Verification of cas no

The CAS Registry Mumber 96859-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,5 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96859-34:
(7*9)+(6*6)+(5*8)+(4*5)+(3*9)+(2*3)+(1*4)=196
196 % 10 = 6
So 96859-34-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N4O/c12-6-3-1-2-5(4-6)7-8-10-11-9-7/h1-4,12H,(H,8,9,10,11)

96859-34-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H27529)  3-(1H-Tetrazol-5-yl)phenol, 97%   

  • 96859-34-6

  • 250mg

  • 532.0CNY

  • Detail
  • Alfa Aesar

  • (H27529)  3-(1H-Tetrazol-5-yl)phenol, 97%   

  • 96859-34-6

  • 1g

  • 1368.0CNY

  • Detail
  • Alfa Aesar

  • (H27529)  3-(1H-Tetrazol-5-yl)phenol, 97%   

  • 96859-34-6

  • 5g

  • 4219.0CNY

  • Detail

96859-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2H-tetrazol-5-yl)phenol

1.2 Other means of identification

Product number -
Other names -

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

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More Details:96859-34-6 SDS

96859-34-6Relevant articles and documents

Magnetic nitrogen-doped carbon derived from silk cocoon biomass: a promising and sustainable support for copper

Akbarzadeh, Parisa,Koukabi, Nadiya,Tahmasbi, Marzieh

, (2021/12/01)

In this study, a magnetic nitrogen-doped carbon-based copper (MNC-Cu) catalyst was fabricated so that natural silk cocoons undergo thermal processes and then activate by combining with Fe3O4 MNPs as a suitable substrate for placement copper metal. The efficiency of the generated catalyst in the synthesis of 5-substituted 1H-tetrazole derivatives was evaluated by the [3 + 2] cycloaddition reaction of aromatic aldehydes, azide ions, and hydroxylamines. FT-IR, FE-SEM, EDS, TEM, XRD, TGA, and VSM techniques have been adopted to identify and validate this heterogeneous catalyst. The observation from EDS, elemental mapping, XRD, and FT-IR analysis confirms the immobilization of Cu metals on the MNC surface and uniform distribution of species and then no aggregation occurs during functionalization. VSM results show the magnetic feature of fabricated catalyst, and based on the leaching test, the amount of catalyst leaching was negligible. Moreover, this reaction is a one-pot multicomponent reaction (MCRs) or more precisely a one-pot, three-component reaction, which is one of the advantages of this work. The fabricated catalyst shows high efficiency, good stability, and considerable reactivity in synthesizing 5-substituted 1H-tetrazole derivatives. So it can be seen that the fabricated magnetic catalyst is a useful and practical catalyst for synthesizing [3 + 2] cycloaddition reactions. Reusability and recyclability for five sequential runs without notable increase and reduction in activity are other advantages. In addition, the magnetic properties of this heterogeneous catalyst led to easy and quickly recovered and striking copper leaching. Graphical abstract: [Figure not available: see fulltext.]

Photophysical and biological investigation of phenol substituted rhenium tetrazolato complexes

Akabar, Nurshadrina,Chaturvedi, Vishal,Shillito, Georgina E.,Schwehr, Bradley J.,Gordon, Keith C.,Huff, Gregory S.,Sutton, Joshua J.,Skelton, Brian W.,Sobolev, Alexandre N.,Stagni, Stefano,Nelson, Delia J.,Massi, Massimiliano

, p. 15613 - 15624 (2019/11/05)

The synthesis, structural and photophysical characterisation of four tricarbonyl rhenium(i) complexes bound to 1,10-phenanthroline and a tetrazolato ancillary ligand are reported. The complexes are differentiated by the nature (hydroxy or methoxy) and pos

A novel method for the synthesis of 5-substituted 1H-tetrazole from oxime and sodium azide

Patil, Umakant B.,Kumthekar, Kedar R.,Nagarkar, Jayashree M.

experimental part, p. 3706 - 3709 (2012/09/21)

A simple and efficient protocol is developed for the synthesis of 5-substituted 1H-tetrazoles from various oximes and sodium azide (NaN 3) by using copper acetate as a catalyst.

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