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N,N-dimethyl-N-(prop-2-yn-1-yl)anilinium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23586-52-9

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23586-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23586-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,8 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23586-52:
(7*2)+(6*3)+(5*5)+(4*8)+(3*6)+(2*5)+(1*2)=119
119 % 10 = 9
So 23586-52-9 is a valid CAS Registry Number.

23586-52-9Downstream Products

23586-52-9Relevant academic research and scientific papers

General Base Catalyzed Hydrogen Exchange of 1-Octyne, 4-Nitrophenylacetylene, and 3-(Phenyldimethylammonio)-1-propyne. Broensted Relations and Normal Acid Behavior

Kresge, A. J.,Powell, M. F.

, p. 822 - 824 (1986)

Rates of loss of tritium from the title compounds labeled at the acetylenic hydrogen position were measured in aqueous primary amine buffer solutions at 25 deg C.These data give Broensted relations with essentially unit exponents: β = 0.97 +/- 0.06 for 1-octyne, β = 0.97 +/- 0.05 for 4-nitrophenylacetylene, and β = 0.98 +/- 0.05 for 3-(phenyldimethylammonio)-1-propyne, which indicates that these acetylenes are "normal" rather than pseudo carbon acids.

Synthesis and properties of an ionic polyacetylene: Poly(dimethylphenylpropargylammonium bromide)

Lee, Won-Chul,Jin, Sung-Ho,Park, Jong-Wook,Lyoo, Won Seok,Gal, Yeong-Soon,Kim, Suhkmann

, p. 158 - 164 (2010)

A monosubstituted ionic polyacetylene having a quaternary ammonium salt was synthesized and characterized. The polymerization of dimethylphenylpropargylammonium bromide (DMPPAB) was performed by various transition metal catalysts to give the resulting pol

Kinetics of the reaction of N,N-dimethylaniline with 1-bromoalk-2-ynes

Andreev,Ryzhakov,Sobolev

, p. 1486 - 1489 (2017/09/01)

Quaternization of N,N-dimethylaniline with propargyl bromide, 1-bromobut-2-yne, and 1-bromooct-2-yne were studied. It was shown that, with the lengthening chain of the substituent at the triple bond, the quaternization rate tends to increase.

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