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(3S,4S)-3-(2-HYDROXY-ETHYL)-3,4-DIHYDRO-2H-PYRAN-4-OL is a dihydropyran derivative with a molecular formula of C6H12O3. It features a hydroxyethyl group attached to the third carbon and a hydroxy group at the fourth carbon. This colorless liquid is soluble in water and is commonly utilized as a key intermediate in the synthesis of pharmaceuticals, fragrances, and flavoring agents. Its potential extends to the development of new drugs and biologically active compounds.

87614-58-2

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87614-58-2 Usage

Uses

Used in Pharmaceutical Research:
(3S,4S)-3-(2-HYDROXY-ETHYL)-3,4-DIHYDRO-2H-PYRAN-4-OL is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure and reactivity.
Used in Fragrance Industry:
(3S,4S)-3-(2-HYDROXY-ETHYL)-3,4-DIHYDRO-2H-PYRAN-4-OL is used as a key intermediate for creating fragrances, leveraging its ability to contribute to the development of novel scents.
Used in Flavor Industry:
(3S,4S)-3-(2-HYDROXY-ETHYL)-3,4-DIHYDRO-2H-PYRAN-4-OL is used as a precursor in the development of new flavoring agents, taking advantage of its potential to enhance or create unique tastes.
Used in Organic Synthesis:
(3S,4S)-3-(2-HYDROXY-ETHYL)-3,4-DIHYDRO-2H-PYRAN-4-OL is used as a versatile intermediate in organic synthesis, allowing for the creation of a wide range of chemical compounds.
Used in Drug Development:
(3S,4S)-3-(2-HYDROXY-ETHYL)-3,4-DIHYDRO-2H-PYRAN-4-OL is used as a potential starting point for the development of new drugs and biologically active compounds, given its unique structural features and solubility properties.

Check Digit Verification of cas no

The CAS Registry Mumber 87614-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87614-58:
(7*8)+(6*7)+(5*6)+(4*1)+(3*4)+(2*5)+(1*8)=162
162 % 10 = 2
So 87614-58-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O3/c8-3-1-6-5-10-4-2-7(6)9/h2,4,6-9H,1,3,5H2/t6-,7+/m0/s1

87614-58-2Relevant academic research and scientific papers

ENANTIOSPECIFIC TOTAL SYNTHESIS OF PSEUDOMONIC ACIDS FROM ARABINOSE

Fleet, G. W. J.,Gough, M. J.,Shing, T. K. M.

, p. 3661 - 3664 (2007/10/02)

The enantiospecific synthesis of pseudomonic acids from arabinose is described.

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