142666-04-4 Usage
General Description
(+)(-)-8,12-trans-9-oxo-prosta-5,14-dienoic acid is a chemical compound belonging to the class of prostaglandins. It is an eicosanoid, which means it is derived from fatty acids and has important physiological functions in the human body. This particular compound is known for its potent inflammatory effects and is involved in the regulation of various processes such as blood pressure, smooth muscle contraction, and immune response. It is also a key player in the pathogenesis of various diseases, including cardiovascular diseases and cancer. Research on this compound has focused on understanding its molecular mechanisms and developing potential therapeutic interventions targeting its biological pathways. Overall, (+)(-)-8,12-trans-9-oxo-prosta-5,14-dienoic acid plays a crucial role in inflammation and is an important target for drug development and disease management.
Check Digit Verification of cas no
The CAS Registry Mumber 142666-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,6,6 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 142666-04:
(8*1)+(7*4)+(6*2)+(5*6)+(4*6)+(3*6)+(2*0)+(1*4)=124
124 % 10 = 4
So 142666-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H32O3/c1-2-3-4-5-6-9-12-17-15-16-19(21)18(17)13-10-7-8-11-14-20(22)23/h6-7,9-10,17-18H,2-5,8,11-16H2,1H3,(H,22,23)/b9-6+,10-7-/t17-,18+/m0/s1
142666-04-4Relevant articles and documents
Synthesis of a preclavulones analogous: (±) 8,12-trans-(5Z,14Z)-9-oxo-prosta-5,10,14-trienoic acid methyl ester via its 10-11 dihydroprecursor from allyl 2-oxo-cyclopentanecarboxylate
Leggeri,Di Giacomo,Papeo,Pirillo,Traverso
, p. 117 - 126 (2007/10/02)
In this paper we report a method to prepare the (±)-8,12-trans(5Z,14Z)-9-oxo-prosta-5,10,14-trienoic acid methyl ester 1, a 11-desoxyprostanoid correlated to the class of Preclavulones, via a new easy synthesis of its 10-11 dihydroprecursor 16 and through a general procedure for the conversion of these 10-11 dihydrocompounds to the unsaturated analogous derivatives.