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1,3,5-Triazin-2(1H)-one, 1,5-dibutyltetrahydro-3-[(4-methylphenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27117-97-1

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27117-97-1 Usage

Type of compound

Heterocyclic compound

Structure

Contains a triazine ring and a sulfonyl group

Substituents

Butyl and methyl phenyl groups

Potential applications

Pharmacological and medicinal

Bioactivity

Structure suggests potential bioactive properties

Further research

Necessary to fully understand potential uses and effects
Please note that this is a brief summary based on the provided material, and further research and testing would be required to fully understand the properties and potential applications of 1,3,5-Triazin-2(1H)-one, 1,5-dibutyltetrahydro-3-[(4-methylphenyl)sulfonyl]-.

Check Digit Verification of cas no

The CAS Registry Mumber 27117-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,1 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27117-97:
(7*2)+(6*7)+(5*1)+(4*1)+(3*7)+(2*9)+(1*7)=111
111 % 10 = 1
So 27117-97-1 is a valid CAS Registry Number.

27117-97-1Downstream Products

27117-97-1Relevant academic research and scientific papers

Mannich reaction of 1-n-butyl-3-p-tosylurea. I. Syntheses of 3-n-butyl-2-oxo-1,5-di-p-tosyl-perhydro-1,3,5-triazine and 3,5-di-n-butyl-2-oxo-1-p-tosyl-perhydro-1,3,5-triazine

Ebi, Godwin C.,Brain, Keith R.,Udeala, Oleka K.

, p. 639 - 641 (1996)

1-n-Butyl-3-p-tosylurea (tolbutamide) does not incorporate the secondary amines, piperidine, diethylamine, dimethylamine, dipropylamine, pyrrolidine and morpholine, to any significant extent in its normal Mannich reaction under alkaline conditions in refluxing methanol, accetonitrile and dioxane. Instead 3-n-butyl-2-oxo-1,5-di-p-tosyl-perhydro-1,3,5-triazine and 3,5-di-n-butyl-2-oxo-1-p-tosyl-perhydro-1,3,5-triazine are mainly formed usually in good yields. These triazines have been isolated and characterized, and a mechanism is proposed for their formation.

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