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2,4,6-trinitrophenol piperidine (1:1) is a chemical compound formed by the combination of 2,4,6-trinitrophenol, also known as picric acid, and piperidine in a one-to-one ratio. It is a yellow crystalline solid with properties that make it relevant in various industries, including pharmaceuticals, agrochemicals, and explosives.

6091-49-2

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6091-49-2 Usage

Uses

Used in Pharmaceutical Industry:
2,4,6-trinitrophenol piperidine (1:1) is used as a precursor in the synthesis of pharmaceuticals for its ability to facilitate the formation of complex organic molecules.
Used in Agrochemical Industry:
2,4,6-trinitrophenol piperidine (1:1) is used as a reagent in the development of agrochemicals, contributing to the creation of effective compounds for agricultural applications.
Used in Explosives Industry:
2,4,6-trinitrophenol piperidine (1:1) is used as a component in the production of explosives due to its properties that enhance the explosive power of certain formulations.
Used in Dyes Industry:
2,4,6-trinitrophenol piperidine (1:1) is used as a precursor in the production of dyes, taking advantage of its color-producing characteristics to create a range of hues for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6091-49-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,9 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6091-49:
(6*6)+(5*0)+(4*9)+(3*1)+(2*4)+(1*9)=92
92 % 10 = 2
So 6091-49-2 is a valid CAS Registry Number.

6091-49-2Downstream Products

6091-49-2Relevant academic research and scientific papers

HYDROGEN BONDED COMPLEXES IV; UREA-PHENOL COMPLEXES

Barry, John E.,Finkelstein, Manuel,Hutchins, Gudrun A.,Ross, Sidney D.

, p. 2151 - 2156 (2007/10/02)

A number of crystalline, hydrogen-bonded complexes of ureas and phenols are reported.The most commonly observed urea-phenol ratio is 1:1, but some complexes with ratios of 2:1, 1:2 and 1:3 were encountered.The structures of these complexes are discussed and one degradative reaction is described.

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