125997-14-0 Usage
Description
1-(3-fluorophenyl)-4-penten-1-ol is a chemical compound characterized by its molecular formula C11H13FO. It is an unsaturated alcohol with a double bond in its structure and features a fluorine atom attached to a phenyl ring. 1-(3-fluorophenyl)-4-penten-1-ol also contains a penten-1-ol moiety, which suggests its potential use as a building block in organic synthesis.
Uses
Used in Medicinal Chemistry:
1-(3-fluorophenyl)-4-penten-1-ol is used as a compound in medicinal chemistry for its potential applications in the development of pharmaceuticals. The presence of a fluorine atom in the structure often leads to enhanced properties in drug candidates, making this compound a promising candidate for further study and development.
Used in Synthetic Chemistry:
1-(3-fluorophenyl)-4-penten-1-ol is used as a building block in synthetic chemistry for the production of other chemical compounds or materials. The penten-1-ol moiety in its structure indicates its potential for use in creating a variety of synthesized products, which may have applications in various industries.
Used in Pharmaceutical Development:
1-(3-fluorophenyl)-4-penten-1-ol is used as a starting material or intermediate in the pharmaceutical industry for the synthesis of new drugs. The unique structure of this compound, including the fluorine atom and the double bond, may provide specific advantages in the design and synthesis of novel pharmaceutical agents.
Used in Chemical Research:
1-(3-fluorophenyl)-4-penten-1-ol is used as a subject of study in chemical research to better understand its properties, reactivity, and potential applications. Further investigation into this compound may reveal additional uses and benefits in various fields, including materials science, environmental chemistry, and more.
Check Digit Verification of cas no
The CAS Registry Mumber 125997-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,9 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 125997-14:
(8*1)+(7*2)+(6*5)+(5*9)+(4*9)+(3*7)+(2*1)+(1*4)=160
160 % 10 = 0
So 125997-14-0 is a valid CAS Registry Number.
125997-14-0Relevant articles and documents
Highly Enantioselective Construction of Dihydrooxazines via Pd-Catalyzed Asymmetric Carboetherification
Li, Na,Sun, Baozhen,Liu, Shuang,Zhao, Jinbo,Zhang, Qian
supporting information, p. 190 - 193 (2020/01/02)
A straightforward synthesis of highly enantioenriched 5,6-dihydro-4H-1,2-oxazines is realized by Pd-catalyzed asymmetric carboetherification of γ,δ-alkenyl oximes with (hetero)aryl and alkenyl halides in the presence of a commercially available bisphosphine ligand. The enantioenriched products can be facilely converted to functionalized alcohols with high fidelity of chiral transfer.
Mechanism of the palladium dichloride catalyzed cope rearrangement of acyclic dienes. A substituent effect study
Overman, Larry E.,Renaldo, Alfred F.
, p. 3945 - 3949 (2007/10/02)
The PdCl2-catalyzed Cope rearrangement of eight 2-aryl-1,5-hexadienes was studied. No simple substituent effect relationship was found, since the catalyzed-rearrangement rate was decreased by introducing both electron-withdrawing and electron-d
