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24852-69-5

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24852-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24852-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,5 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24852-69:
(7*2)+(6*4)+(5*8)+(4*5)+(3*2)+(2*6)+(1*9)=125
125 % 10 = 5
So 24852-69-5 is a valid CAS Registry Number.

24852-69-5Relevant academic research and scientific papers

NOVEL METHOD FOR PREPARING SELENYL-SUBSTITUTED AROMATIC ALDEHYDE COMPOUNDS

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Paragraph 0180-0182, (2017/07/31)

The present invention relates to a novel method for preparing selenyl-substituted aromatic aldehyde compounds. More specifically, the method comprises the step of forming selenolate nucleophile and performing nucleophilic substitution of selenyl-substitut

NOVEL METHOD FOR PREPARING SELENYL-SUBSTITUTED AROMATIC ALDEHYDE COMPOUNDS

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Paragraph 0174-0176; 0182, (2016/10/10)

A, [...] -substituted aromatic aldehydes (selenyl-substituted aromatic aldehyde) compound relates to novel manufacturing method, specifically, form (selenolate nucleophile) nucleophile [...] aromatic aldehyde-based starting material including the nucleoph

NOVEL METHOD FOR PREPARING SELENYL-SUBSTITUTED AROMATIC ALDEHYDE COMPOUNDS

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Paragraph 0096; 0097; 0098, (2014/02/15)

The present disclosure relates to a novel method for preparing selenyl-substituted aromatic aldehyde compounds by forming a selenolate nucleophile and performing a nucleophilic substitution reaction between the selenolate nucleophile and an aromatic aldeh

Mild generation of selenolate nucleophiles by thiol reduction of diselenides: Convenient syntheses of selenyl-substituted aryl aldehydes

Dubey, Rashmi,Lee, Hangeun,Nam, Do-Hyun,Lim, Dongyeol

experimental part, p. 6839 - 6842 (2012/01/04)

Various selenyl-substituted aryl aldehydes were obtained using dithiothreitol (DTT) as a reducing agent for diselenides in the presence of a base. For electron-deficient haloaryl aldehydes, a weak base, such as K 2CO3, performed well. However, for electron-rich haloaryl aldehydes, a stronger base, such as 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), was required for successful substitution. The selenyl-substitution of heteroaryl substrates were also investigated to obtain satisfactory yields of the desired products.

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