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1-Propanone, 3-(dimethylamino)-1,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24686-81-5

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24686-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24686-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,8 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24686-81:
(7*2)+(6*4)+(5*6)+(4*8)+(3*6)+(2*8)+(1*1)=135
135 % 10 = 5
So 24686-81-5 is a valid CAS Registry Number.

24686-81-5Relevant academic research and scientific papers

Preparation method and application of cross-linked acid system high-temperature-resistant acidizing corrosion inhibitor

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Paragraph 0040; 0055-0056; 0061- 0062; 0066-0067, (2020/08/22)

The invention relates to a preparation method and application of a cross-linked acid system high-temperature-resistant acidizing corrosion inhibitor. The preparation method comprises the following steps: respectively adding an aldehyde monomer, a ketone monomer and an amine monomer into a reactor; performing dispersing with absolute ethyl alcohol; and performing reacting at a temperature of 60-100DEG C to obtain Mannich base; and after the system is cooled, adding halogenated alkane, and continuously reacting at a temperature of 60-100 DEG C to obtain a Mannich base quaternary ammonium salt corrosion inhibitor. The obtained Mannich base quaternary ammonium salt corrosion inhibitor can be directly used without purification. The acidizing corrosion inhibitor provided by the invention has better temperature resistance and compatibility, is used at a high temperature of 180 DEG C, and is suitable for various processes of oil field acidizing construction.

Alkoxide activation of aminoboranes towards selective amination

Sole, Cristina,Fernandez, Elena

supporting information, p. 11351 - 11355 (2013/11/06)

Piece of the (inter)action: The interaction of alkoxides with the sp 2 Bpin (pin=pinacol) moiety in aminoboranes forms the in situ Lewis acid-base adduct [RO-→B(OR)2-N(R′)2] which enables the amino moiety to react as a strong nucleophile with several electrophiles, thus providing amino alcohols, β-enamino esters, and β-hydroxy amides in a direct and remarkably selective way (see scheme). Copyright

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