254891-67-3 Usage
General Description
2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)- (9CI) is a chemical compound with the molecular formula C8H10O. It is a derivative of furanmethanol and contains an ethynyl group, as well as a tetrahydrofuran ring. 2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)- (9CI) is classified as a chiral molecule due to its asymmetric carbon centers at positions 2 and 5. It is commonly used in organic synthesis and chemical research due to its unique structural features. 2-Furanmethanol, 5-ethynyltetrahydro-, (2S,5S)- (9CI) may have potential pharmaceutical or industrial applications, and its properties and reactivity are of interest to chemists and researchers.
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.
