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873-62-1

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873-62-1 Usage

Description

3-Cyanophenol, also known as 3-Hydroxybenzonitrile, is an organic compound characterized by the presence of a hydroxyl group and a nitrile group attached to a benzene ring. It exhibits unique chemical properties due to the presence of these functional groups, making it a versatile intermediate in organic synthesis.

Uses

Used in Pharmaceutical Industry:
3-Cyanophenol is used as an intermediate in the synthesis of new Serotonin 5-HT1A receptor agonists, which possess antinociceptive activity in vivo. These agonists have potential applications in the development of medications for pain management and other related therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 873-62-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 873-62:
(5*8)+(4*7)+(3*3)+(2*6)+(1*2)=91
91 % 10 = 1
So 873-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NO/c8-5-6-2-1-3-7(9)4-6/h1-4,9H

873-62-1 Well-known Company Product Price

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  • Alfa Aesar

  • (B21702)  3-Hydroxybenzonitrile, 99%   

  • 873-62-1

  • 5g

  • 521.0CNY

  • Detail
  • Alfa Aesar

  • (B21702)  3-Hydroxybenzonitrile, 99%   

  • 873-62-1

  • 25g

  • 2359.0CNY

  • Detail

873-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxybenzonitrile

1.2 Other means of identification

Product number -
Other names 3-Cyanophenol

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:873-62-1 SDS

873-62-1Relevant articles and documents

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Smith

, p. 221 (1877)

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Transforming a Fluorochrome to an Efficient Photocatalyst for Oxidative Hydroxylation: A Supramolecular Dimerization Strategy Based on Host-Enhanced Charge Transfer

Tang, Bohan,Xu, Weiquan,Xu, Jiang-Fei,Zhang, Xi

supporting information, p. 9384 - 9388 (2021/03/22)

The development of non-covalent synthetic strategy to fabricate efficient photocatalysts is of great importance in theranostic and organic materials. Herein, a fluorochrome N,N′-dimethyl 2,5-bis(4-pyridinium)thiazolo[5,4-d]thiazolediiodide (MPT) was transformed into an efficient photocatalyst through supramolecular dimerization in the cavity of cucurbit[8]uril (CB[8]). The host-enhanced charge transfer interaction within the supramolecular dimer 2MPT-CB[8] dramatically promoted intersystem crossing to produce triplet. In addition, the staggered conformation of 2MPT-CB[8] facilitated the energy transfer and electron transfer of the triplet. As a result, 2MPT-CB[8] could serve as a high-efficiency photocatalyst for the oxidative hydroxylation of arylboronic acids. This supramolecular dimerization strategy enriches the supramolecular engineering of functional π-systems. It is anticipated that this strategy can be extended to fabricate various π-systems with tailor-made functions.

Highly Efficient Oxidative Cyanation of Aldehydes to Nitriles over Se,S,N-tri-Doped Hierarchically Porous Carbon Nanosheets

Hua, Manli,Song, Jinliang,Huang, Xin,Liu, Huizhen,Fan, Honglei,Wang, Weitao,He, Zhenhong,Liu, Zhaotie,Han, Buxing

supporting information, p. 21479 - 21485 (2021/08/23)

Oxidative cyanation of aldehydes provides a promising strategy for the cyanide-free synthesis of organic nitriles. Design of robust and cost-effective catalysts is the key for this route. Herein, we designed a series of Se,S,N-tri-doped carbon nanosheets with a hierarchical porous structure (denoted as Se,S,N-CNs-x, x represents the pyrolysis temperature). It was found that the obtained Se,S,N-CNs-1000 was very selective and efficient for oxidative cyanation of various aldehydes including those containing other oxidizable groups into the corresponding nitriles using ammonia as the nitrogen resource below 100 °C. Detailed investigations revealed that the excellent performance of Se,S,N-CNs-1000 originated mainly from the graphitic-N species with lower electron density and synergistic effect between the Se, S, N, and C in the catalyst. Besides, the hierarchically porous structure could also promote the reaction. Notably, the unique feature of this metal-free catalyst is that it tolerated other oxidizable groups, and showed no activity on further reaction of the products, thereby resulting in high selectivity. As far as we know, this is the first work for the synthesis of nitriles via oxidative cyanation of aldehydes over heterogeneous metal-free catalysts.

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