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21598-08-3

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  • Benzooxazole-2-carboxylic acid (Potassium 1,3-benzoxazole-2-carboxylate;sodium benzo[d]oxazole-2-carboxylate ),cas:21598-08-3 from fandachem

    Cas No: 21598-08-3

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21598-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21598-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21598-08:
(7*2)+(6*1)+(5*5)+(4*9)+(3*8)+(2*0)+(1*8)=113
113 % 10 = 3
So 21598-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8FN.ClH/c9-8-3-1-2-6-4-10-5-7(6)8;/h1-3,10H,4-5H2;1H

21598-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-benzoxazole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Benzoxazolecarboxylicacid

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:21598-08-3 SDS

21598-08-3Relevant articles and documents

CO2-Folded Single-Chain Nanoparticles as Recyclable, Improved Carboxylase Mimics

Chen, Liang,Yan, Qiang,Zeng, Rongjin

supporting information, p. 18418 - 18422 (2020/08/21)

Emulating the function of natural carboxylases to convert CO2 under atmospheric condition is a great challenge. Herein we report a class of CO2-folded single-chain nanoparticles (SCNPs) that can function as recyclable, function-intensified carboxylase mimics. Lewis pair polymers containing bulky Lewis acidic and basic groups as the precursor, can bind CO2 to drive an intramolecular folding into SCNPs, in which CO2 as the folded nodes can form gas-bridged bonds. Such bridging linkages highly activate CO2, which endows the SCNPs with extraordinary catalytic ability that can not only catalyze CO2-insertion of C(sp3)-H for imitating the natural enzyme's function, it can also act on non-natural carboxylation pathways for C(sp2 and sp)-H substrates. The nanocatalysts are of highly catalytic efficiency and recyclability, and can work at room temperature and near ambient CO2 condition, inspiring a new approach to sustainable C1 utilization.

Direct C-H carboxylation with carbon dioxide using 1,2,3-triazol-5-ylidene copper(I) complexes

Inomata, Hiroshi,Ogata, Kenichi,Fukuzawa, Shin-Ichi,Hou, Zhaomin

supporting information; experimental part, p. 3986 - 3989 (2012/09/10)

1,2,3-Triazol-5-ylidene copper(I) complexes (tzNHC-Cu) efficiently catalyzed the direct C-H carboxylation of benzoxazole and benzothiazole derivatives with CO2 to give the corresponding esters in excellent yields after treatment with alkyl iodi

Carboxylation of N-H/C-H bonds using n-heterocyclic carbene copper(I) complexes

Boogaerts, Ine I. F.,Fortman, George C.,Furst, Marc R. L.,Cazin, Catherine S. J.,Nolan, Steven P.

supporting information; scheme or table, p. 8674 - 8677 (2011/01/06)

Greenhouse gas makes good: A simple copper-mediated protocol has been developed where N-H or C-H bonds can be directly functionalized using an easily prepared catalyst. The novel [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene] copper(I) hydroxide, [Cu(IPr)(OH)], permits the facile activation and carboxylation of N-H and C-H bonds with pKavalues of less than 27.7 (see scheme).

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