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4743-58-2

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4743-58-2 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 15, p. 627, 1950 DOI: 10.1021/jo01149a028

Check Digit Verification of cas no

The CAS Registry Mumber 4743-58-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,4 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4743-58:
(6*4)+(5*7)+(4*4)+(3*3)+(2*5)+(1*8)=102
102 % 10 = 2
So 4743-58-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O4/c11-9(12)5-8-6-3-1-2-4-7(6)10(13)14-8/h1-4,8H,5H2,(H,11,12)

4743-58-2 Well-known Company Product Price

  • Brand
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  • Alfa Aesar

  • (L05984)  Phthalide-3-acetic acid, 98+%   

  • 4743-58-2

  • 5g

  • 408.0CNY

  • Detail
  • Alfa Aesar

  • (L05984)  Phthalide-3-acetic acid, 98+%   

  • 4743-58-2

  • 25g

  • 1457.0CNY

  • Detail

4743-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Phthalide-3-Acetic Acid

1.2 Other means of identification

Product number -
Other names 2-(3-oxo-1H-2-benzofuran-1-yl)acetic acid

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:4743-58-2 SDS

4743-58-2Relevant articles and documents

Hydroperoxide oxidation of different organic compounds catalyzed by silica-supported selenenamide

Giurg,Brzaszcz,Mlochowski

, p. 417 - 428 (2007/10/03)

The recoverable heterogeneous silica-supported catalyst selenenamide 2 was prepared by the coupling of 3-aminopropylsilicate (4) with 2-chloroselenobenzoyl chloride (6). Its catalytic activity was demonstrated in tert-butyl hydroperoxide oxidation of aldehydes 8 to carboxylic acids 9 and benzylamines 17 to nitriles 18. Moreover, it was employed for hydrogen peroxide oxidation of azomethine compounds such as tosylhydrazones 10, oximes 13 and N,N-dimethylhydrazones 16 to parent ketones 12, arenecarboxylic acids 11 and 15, their methyl esters 14 and nitriles 18 depending on the substrate used and the reaction conditions. The catalyst was simply recovered by filtration and could be reused.

One-pot oxidation of azomethine compounds into arenecarboxylic acids

Giurg,Said,Syper,Mlochowski

, p. 3151 - 3159 (2007/10/03)

Aromatic azomethine compounds, such as aldazines 1, aldoximes 7 and tosylhydrazones 8 oxidized with 30% hydrogen peroxide in the presence of poly(bis-1,2-phenylene) diselenide (6) as catalyst produce arenecarboxylic acids 2 mostly in high to excellent yields. The presented one-pot procedure has a synthetic value.

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