94595-91-2 Usage
Description
(3aS,4S,5R,6aR)-Hexahydro-5-hydroxy-4-(hydroxyMethyl)-2(1H)-pentalenone is a complex organic compound that features a six-membered ring system with a ketone functional group and two hydroxyl groups. It is a pentalenone derivative, which is often found in nature. This specific compound is characterized by a hydroxymethyl group attached to the carbon adjacent to the ketone, endowing it with unique chemical properties. Its distinctive structure makes it a promising candidate for further study and potential applications in medicinal chemistry and as a building block for the synthesis of other organic compounds.
Uses
Used in Medicinal Chemistry:
(3aS,4S,5R,6aR)-Hexahydro-5-hydroxy-4-(hydroxyMethyl)-2(1H)-pentalenone is used as a potential compound in medicinal chemistry due to its unique chemical properties and structural features. Its hydroxymethyl group and ketone functional group may contribute to its interaction with biological targets, making it a candidate for the development of new pharmaceuticals.
Used in Organic Synthesis:
In the field of organic synthesis, (3aS,4S,5R,6aR)-Hexahydro-5-hydroxy-4-(hydroxyMethyl)-2(1H)-pentalenone serves as a building block for the synthesis of other complex organic compounds. Its unique structure allows for further chemical modifications and reactions, facilitating the creation of novel molecules with potential applications in various industries.
Used in Research and Development:
(3aS,4S,5R,6aR)-Hexahydro-5-hydroxy-4-(hydroxyMethyl)-2(1H)-pentalenone is utilized in research and development settings to explore its chemical properties and potential applications. Its distinctive structure makes it an interesting target for scientists to study and understand its behavior in different chemical environments, which could lead to new discoveries and applications in science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 94595-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 94595-91:
(7*9)+(6*4)+(5*5)+(4*9)+(3*5)+(2*9)+(1*1)=182
182 % 10 = 2
So 94595-91-2 is a valid CAS Registry Number.
94595-91-2Relevant articles and documents
Synthesis and anti-platelet aggregating activity of 3-hetero analogues of (+)-9(O)-methano-Δ(6(9α))-prostaglandin I1
Kojima,Amemiya,Koyama,Saito,Oshima,Ito
, p. 4000 - 4015 (2007/10/02)
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STEREOCHEMICAL STUDIES - LVII. SYNTHESIS OF OPTICALLY ACTIVE COMPOUNDS BY THE NOVEL USE OF MESO-COMPOUNDS -1. EFFICIENT SYNTHESIS OF TWO STRUCTURAL TYPES OF OPTICALLY PURE PROSTAGLANDIN INTERMEDIATES.
Nara, M,Terashima, S.,Yamada, S.
, p. 3161 - 3170 (2007/10/02)
With an aim to overcome several inefficient aspects of ordinary methods of preparing optically active compounds, we have developed a new method which recommends utilization of symmetrically functionalized meso-compounds in place of racemic compounds.As shown in Scheme 1, when the meso-compound (I) is monofunctionalized by an optically active functional group (A) and each of the formed diastereomers (II and III) is subjected to further chemical elaborations including protective group transposition, it is theoretically possible to convert the total amount of the starting material (I) into the requisite optically pure product (VI or VII) by selecting synthetic schemes.By employing this novel concept, two structural types of the prostaglandin intermediates ((-)- and (+)-2a,b) have been prepared from the meso-diols (1a,b) by way of the two diastereomeric monoesters (13a,b and 14a,b) which are produced by the reactions 1a,b with N-mesyl- and N-phthaloyl-(S)-phenylalanyl chloride (3a,b).
