1430731-70-6 Usage
Molecular structure
2,2-bis(hydroxymethyl)propyl (5Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-5-phenyl-1-pentenyl]cyclopentyl]-5-heptenoate is a complex molecule with multiple functional groups and stereocenters.
Functional groups
The compound contains hydroxyl groups (-OH), a cyclopentyl ring (C5H9), and a heptenoate ester (C7H11O2).
Potential therapeutic applications
Due to the presence of hydroxyl groups and a phenyl moiety (C6H5), 2,2-bis(hydroxymethyl)propyl (5Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-5-phenyl-1-pentenyl]cyclopentyl]-5-heptenoate may have pharmacological properties. The hydroxyl groups can form hydrogen bonds, which are essential for many biological processes, while the phenyl group can contribute to the compound's solubility and stability.
Need for further research
Although the compound appears to have potential therapeutic applications, more research is needed to fully understand its biological activity and potential uses. This includes studying its interactions with biological targets, toxicity, and efficacy in preclinical models.
Check Digit Verification of cas no
The CAS Registry Mumber 1430731-70-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,0,7,3 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1430731-70:
(9*1)+(8*4)+(7*3)+(6*0)+(5*7)+(4*3)+(3*1)+(2*7)+(1*0)=126
126 % 10 = 6
So 1430731-70-6 is a valid CAS Registry Number.
1430731-70-6Relevant articles and documents
PROCESS FOR PREPARATION OF PROSTAGLANDIN F2 ALPHA ANALOGUES
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Paragraph 0282, (2015/02/19)
A convergent synthesis of the prostaglandin F2α analogues, travoprost and bimatoprost, was developed employing Julia-Lythgoe olefination of the structurally advanced phenylsulfone with an enantiomerically pure aldehyde ω-chain synthon. The novel convergent strategy allows the synthesis of a whole series of prostaglandin analogues of high purity from a common and structurally advanced prostaglandin intermediate.
PROCESS FOR PREPARATION OF PROSTAGLANDIN F2α ANALOGUES
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, (2013/09/26)
A convergent synthesis of the prostaglandin F2α analogues, travoprost and bimatoprost, was developed employing Julia-Lythgoe olefination of the structurally advanced phenylsulfone with an enantiomerically pure aldehyde ω-chain synthon. The novel convergent strategy allows the synthesis of a whole series of prostaglandin analogues of high purity from a common and structurally advanced prostaglandin intermediate.
A novel convergent synthesis of the antiglaucoma PGF2α analogue bimatoprost
Dams, Iwona,Chodyński, Micha?,Krupa, Ma?gorzata,Pietraszek, Anita,Zezula, Marta,Cmoch, Piotr,Kosińska, Monika,Kutner, Andrzej
, p. 170 - 179 (2013/08/25)
The 17-phenyl PGF2α analogue bimatoprost (10a) is the most efficacious ocular hypotensive agent currently available for the treatment of glaucoma or ocular hypertension. A novel convergent synthesis of 13,14-en-15-ol prostamideF2α an
