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2-Furanol, 5-cyclohexyltetrahydro-4-[(4-methylphenyl)sulfonyl]is a heterocyclic chemical compound characterized by a complex structure that includes a furan ring and a sulfonyl group. 2-Furanol, 5-cyclohexyltetrahydro-4-[(4-methylphenyl)sulfonyl]is commonly utilized in pharmaceutical and chemical research due to its unique structural features and reactivity.
Used in Pharmaceutical Research:
2-Furanol, 5-cyclohexyltetrahydro-4-[(4-methylphenyl)sulfonyl]is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential role in the development of new drugs. Its structural features and reactivity make it a promising candidate for creating novel therapeutic agents.
Used in Chemical Research:
In the field of chemical research, 2-Furanol, 5-cyclohexyltetrahydro-4-[(4-methylphenyl)sulfonyl]is employed as a versatile building block for the creation of complex organic molecules. Its unique properties allow for the exploration of new chemical reactions and the synthesis of innovative materials.
It is crucial to handle 2-Furanol, 5-cyclohexyltetrahydro-4-[(4-methylphenyl)sulfonyl]with care and to follow proper safety protocols when working with it in laboratory settings to ensure the safety of researchers and the integrity of experiments.

146174-48-3

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146174-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146174-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,7 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 146174-48:
(8*1)+(7*4)+(6*6)+(5*1)+(4*7)+(3*4)+(2*4)+(1*8)=133
133 % 10 = 3
So 146174-48-3 is a valid CAS Registry Number.

146174-48-3Relevant academic research and scientific papers

(Alkoxyallyl)sulfones as enal β-anion equivalents. Synthesis of 5-substituted 2(5H)-furanones

Craig, Donald,Etheridge, Christopher J.,Smith, Alison M.

, p. 15267 - 15288 (2007/10/03)

2(5H)-Furanones 14 may be prepared in a four-step sequence starting from (alkoxyallyl)sulfone 10 and aldehydes.

1-Benzyloxy-3-(p-tolylsulfonyl)propene as an acrolein β-anion equivalent. Synthesis of 4-substituted 2-butenolides

Craig, Donald,Etheridge, Christopher J.,Smith, Alison M.

, p. 7445 - 7446 (2007/10/02)

Lithiation of 1-benzyloxy-3-(p-tolylsulfonyl)propene 6 and reaction with aldehydes give alcohols 7. Sequential hydrolysis-cyclization, oxidation and DBU-mediated elimination of dine elements of p-TolSO2H gives 4-substituted 2-butenolides 10 in good overall yield.

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