39647-93-3 Usage
Description
(S)-trans-3-Hydroxy-1-iodo-1-octene, with the molecular formula C8H15IO, is a chiral chemical compound that exists in two mirror-image forms. The specific form mentioned here is characterized by its unique arrangement of a hydroxy group, an iodine atom, and a double bond within its structure. (S)-trans-3-Hydroxy-1-iodo-1-octene is predominantly utilized as a synthetic intermediate in the realm of organic chemistry, playing a crucial role in the synthesis of an array of pharmaceuticals and agrochemicals. Moreover, it has garnered interest for its prospective applications in the fields of organic synthesis and material science, showcasing its versatility and potential for further research and development.
Uses
Used in Pharmaceutical Industry:
(S)-trans-3-Hydroxy-1-iodo-1-octene is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structural features allow it to serve as a key component in the creation of novel drugs, contributing to the advancement of medical treatments and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-trans-3-Hydroxy-1-iodo-1-octene is employed as a synthetic intermediate for the production of different agrochemicals. Its incorporation aids in the synthesis of innovative compounds that can enhance agricultural productivity and contribute to more effective pest control solutions.
Used in Organic Synthesis:
(S)-trans-3-Hydroxy-1-iodo-1-octene is used as a valuable building block in organic synthesis. Its distinct structural elements make it an attractive candidate for the development of new organic compounds, potentially leading to breakthroughs in various chemical applications.
Used in Material Science:
(S)-trans-3-Hydroxy-1-iodo-1-octene is also utilized in material science research, where its unique properties are investigated for potential applications in the development of new materials with enhanced characteristics. This can include improvements in areas such as conductivity, strength, or responsiveness to environmental stimuli.
Check Digit Verification of cas no
The CAS Registry Mumber 39647-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,4 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39647-93:
(7*3)+(6*9)+(5*6)+(4*4)+(3*7)+(2*9)+(1*3)=163
163 % 10 = 3
So 39647-93-3 is a valid CAS Registry Number.
39647-93-3Relevant articles and documents
A highly efficient synthesis of prostaglandin intermediates possessing the 15S configuration
Noyori,Tomino,Nishizawa
, p. 5843 - 5844 (1979)
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Synthesis of a pyrazole prostacyclin
Suzuki,Sugiura,Noyori
, p. 4817 - 4820 (1982)
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Fully stereocontrolled syntheses of 3-oxacarbacyclin and carbacyclin by the conjugate addition-azoalkene-asymmetric olefination strategy
Kim, Mikhail,Gais, Hans-Joachim
, p. 4642 - 4650 (2007/10/03)
A fully stereocontrolled synthesis of 3-oxacarbacyclin (3) and a formal synthesis of carbacyclin (2) are described. The syntheses are based on the conjugate addition-azoalkene-asymmetric olefination strategy. Its key features are (1) the stereoselective e
Catalytic Asymmetric Addition of Polyfunctional Dialkylzincs to β-Stannylated and β-Silylated Unsaturated Aldehydes
Ostwald, Roswitha,Chavant, Pierre-Yves,Stadtmueller, Heinz,Knochel, Paul
, p. 4143 - 4153 (2007/10/02)
The addition of functionalized dialkylzincs to readily available β-stannylated or β-silylated unsaturated aldehydes in the presence of a catalytic amount of (1R,2R)-1,2-bis(trifluorosulfonamido)cyclohexane (8 mol percent) provides chiral allylic alcohols
