99901-98-1 Usage
Description
(2-bromophenyl)(furan-3-yl)methanol is a chemical compound that consists of a bromophenyl group attached to a furan-3-yl group, both connected to a methanol molecule. It is commonly used in organic synthesis and medicinal chemistry due to its versatile reactivity and potential pharmacological properties.
Uses
Used in Pharmaceutical Chemistry:
(2-bromophenyl)(furan-3-yl)methanol is used as a building block for the development of new drugs due to its unique structure and potential bioactivities.
Used in Organic Synthesis:
(2-bromophenyl)(furan-3-yl)methanol is used as a versatile reagent in organic synthesis for the creation of various chemical compounds.
Used in Antifungal Applications:
(2-bromophenyl)(furan-3-yl)methanol is used as an antifungal agent for its potential to inhibit fungal growth.
Used in Antibacterial Applications:
(2-bromophenyl)(furan-3-yl)methanol is used as an antibacterial agent for its potential to inhibit bacterial growth.
Used in Enzyme Inhibition:
(2-bromophenyl)(furan-3-yl)methanol is used as an enzyme inhibitor for its potential to inhibit certain enzymes, which can be beneficial in treating various diseases.
Used in Synthesis of Biologically Active Compounds:
(2-bromophenyl)(furan-3-yl)methanol is used as a starting material in the synthesis of biologically active compounds, which can have potential applications in medicine and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 99901-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,0 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 99901-98:
(7*9)+(6*9)+(5*9)+(4*0)+(3*1)+(2*9)+(1*8)=191
191 % 10 = 1
So 99901-98-1 is a valid CAS Registry Number.
99901-98-1Relevant articles and documents
Asymmetric Synthesis of 1,2-Dihydronaphthalene-1-ols via Copper-Catalyzed Intramolecular Reductive Cyclization
Acharyya, Ranjan Kumar,Kim, Soyoung,Park, Yeji,Han, Jung Tae,Yun, Jaesook
supporting information, p. 7897 - 7902 (2020/11/02)
We describe a copper-catalyzed intramolecular reductive cyclization of easily accessible benz-tethered 1,3-dienes containing a ketone moiety. This process provided biologically active 1,2-dihydronaphthalene-1-ol derivatives in good yields with excellent enantio- and diastereoselectivity. Mechanistic investigations using density functional theory revealed that (Z)- and (E)-allylcopper intermediates formed in situ from the diene and copper catalyst undergo isomerization and selective intramolecular allylation of the (E)-allylcopper form of the major product through a six-membered boatlike transition state. The resulting products were further transformed to fully saturated naphthalene-1-ols by reactions of the olefin moiety.
Anodic Cyclizations, Seven-Membered Rings, and the Choice of Radical Cation vs. Radical Pathways
Perkins, Robert J.,Feng, Ruozhu,Lu, Qingquan,Moeller, Kevin D.
, p. 672 - 678 (2019/05/28)
While many steps in an oxidative cyclization reaction can be important, it is the cyclization step itself that plays the central role. If this step does not proceed well, then optimization of the rest of the sequence is futile. We report here that the key
