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2-Furanpentanol, tetrahydro-5-hydroxy-3-[(4-methylphenyl)sulfonyl]is a chemical compound with the molecular formula C15H20O5S. It is a tetrahydrofuran derivative that contains a hydroxy group and a sulfonyl group.
Used in Pharmaceutical Industry:
2-Furanpentanol, tetrahydro-5-hydroxy-3-[(4-methylphenyl)sulfonyl]is used as a building block for the synthesis of various drug molecules. It is utilized in the development of new medicines and in chemical research.
Used in Chemical Research:
2-Furanpentanol, tetrahydro-5-hydroxy-3-[(4-methylphenyl)sulfonyl]is used as a research compound for studying its properties and potential applications in the development of new chemical entities.
Used in Fine Chemicals Production:
2-Furanpentanol, tetrahydro-5-hydroxy-3-[(4-methylphenyl)sulfonyl]may have applications in the production of fine chemicals, where its unique structure and functional groups can be utilized for the synthesis of specialty chemicals.
Used in Specialty Materials Production:
2-Furanpentanol, tetrahydro-5-hydroxy-3-[(4-methylphenyl)sulfonyl]may also have potential uses in the production of specialty materials, where its unique properties can be leveraged for the development of new materials with specific characteristics.

185812-05-9

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185812-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185812-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,8,1 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 185812-05:
(8*1)+(7*8)+(6*5)+(5*8)+(4*1)+(3*2)+(2*0)+(1*5)=149
149 % 10 = 9
So 185812-05-9 is a valid CAS Registry Number.

185812-05-9Relevant 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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