88277-19-4 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 4-((1S,2R,3aS,8bS)-2-hydroxy-1-(hydroxymethyl)-2,3,3a,8b-tetrahydro-1Hbenzo[b]cyclopenta[d]furan-5-yl)butanoate is used as an intermediate in the synthesis of pharmaceutical compounds for its potential medicinal properties.
Used in Flavoring and Fragrance Industry:
Methyl 4-((1S,2R,3aS,8bS)-2-hydroxy-1-(hydroxymethyl)-2,3,3a,8b-tetrahydro-1Hbenzo[b]cyclopenta[d]furan-5-yl)butanoate is used as a flavoring agent and fragrance ingredient due to its unique chemical structure that can contribute to the development of novel scents and tastes.
Used in Organic Synthesis:
Methyl 4-((1S,2R,3aS,8bS)-2-hydroxy-1-(hydroxymethyl)-2,3,3a,8b-tetrahydro-1Hbenzo[b]cyclopenta[d]furan-5-yl)butanoate is used as a building block in organic synthesis for the creation of more complex molecules and compounds with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 88277-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,7 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88277-19:
(7*8)+(6*8)+(5*2)+(4*7)+(3*7)+(2*1)+(1*9)=174
174 % 10 = 4
So 88277-19-4 is a valid CAS Registry Number.
88277-19-4Relevant academic research and scientific papers
Total synthesis of optically active m-phenylene PGl2 derivative: Beraprost
Wakita, Hisanori,Yoshiwara, Hideo,Nishiyama, Hisao,Nagase, Hiroshi
, p. 1085 - 1110 (2007/10/03)
The optical isomers of m-phenylene PGl2 derivative, Beraprost, were synthesized in practical scales from optically active carboxy- cyclopenta[b]benzofurans (12 and 13) by Wittig and Wadsworth reactions as key reactions via the intermediate diols (16a and 16b).
Synthesis of (+)-5,6,7-trinor-4,8-inter-m-phenylene PGI2
Nagase, Hiroshi,Matsumoto, Kazuhisa,Yoshiwara, Hideo,Tajima, Atsuko,Ohno, Kiyotaka
, p. 4493 - 4494 (2007/10/02)
The titled compound, which is a stable and potent analog of prostacyclin, was synthesized from readily available 1,4-dibromocyclopentene via cyclopenta[b]benzofuran carboxylic acid 5.
