254891-67-3 Usage
Description
2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)(9CI) is a chiral chemical compound with the molecular formula C8H10O. It is a derivative of furanmethanol, featuring an ethynyl group and a tetrahydrofuran ring. 2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)(9CI) is classified as chiral due to its asymmetric carbon centers at positions 2 and 5, which contribute to its unique structural features. Its properties and reactivity make it a valuable compound in organic synthesis and chemical research.
Uses
Used in Organic Synthesis:
2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)(9CI) is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structural features, including the ethynyl group and tetrahydrofuran ring, make it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Research:
2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)(9CI) is utilized in chemical research to study its properties and reactivity. Researchers are interested in understanding how the asymmetric carbon centers and the presence of the ethynyl group and tetrahydrofuran ring affect its behavior in chemical reactions. This knowledge can contribute to the development of new synthetic methods and the discovery of novel compounds with potential applications.
Used in Pharmaceutical Development:
2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)(9CI) may have potential pharmaceutical applications due to its unique structure and reactivity. It could serve as a key intermediate in the development of new drugs or as a chiral auxiliary in the synthesis of enantiomerically pure compounds, which are often required for biological activity.
Used in Industrial Applications:
2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)(9CI) may also find use in various industrial applications, such as the production of specialty materials, fragrances, or flavorings, where its unique structural features can provide specific properties or reactivity needed for these products.
Check Digit Verification of cas no
The CAS Registry Mumber 254891-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,8,9 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 254891-67:
(8*2)+(7*5)+(6*4)+(5*8)+(4*9)+(3*1)+(2*6)+(1*7)=173
173 % 10 = 3
So 254891-67-3 is a valid CAS Registry Number.
254891-67-3Relevant articles and documents
Stereoselective syntheses of pharmaceutically relevant chiral tetrahydrofurans from (S)- and (R)-glyceraldehyde derivatives
Sharma,Punna, Sreenivas,Rajendra Prasad,Krishna, Palakodety Radna,Chorghade, Mukund S.,Ley, Steven V.
, p. 1113 - 1123 (2007/10/03)
A practically simple and flexible method of making chiral tetrahydrofurans of therapeutic relevance is reported from glyceraldehyde derivatives as chiral synthons. One of the stereocentres is derived from glyceraldehyde derivatives, while the other one is introduced by Sharpless asymmetric epoxidation using either (+)- or (-)-DIPT.
