103594-29-2 Usage
Description
[1,1-Biphenyl]-4-ol,4-methoxy-3-methyl-(9CI), also known as 4-Methoxy-3-methylbiphenyl-4-ol, is an organic compound with the molecular formula C14H14O2. It is a derivative of biphenyl, featuring a methyl and methoxy group attached to the 4th and 3rd positions, respectively. [1,1-Biphenyl]-4-ol,4-methoxy-3-methyl-(9CI) is utilized in the production of a variety of industrial and commercial products and is recognized for its potential biological and pharmacological activities, making it a significant subject of interest for research and development.
Uses
Used in Pharmaceutical Industry:
[1,1-Biphenyl]-4-ol,4-methoxy-3-methyl-(9CI) is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, targeting specific medical conditions.
Used in Fragrance Industry:
In the fragrance industry, [1,1-Biphenyl]-4-ol,4-methoxy-3-methyl-(9CI) is used as a component in the creation of various scent profiles. Its distinct chemical structure contributes to the development of unique and complex fragrances.
Used in Organic Compounds Production:
[1,1-Biphenyl]-4-ol,4-methoxy-3-methyl-(9CI) is also utilized in the production of other organic compounds, serving as a building block for the synthesis of various chemicals used in different industries.
Used in Research and Development:
Due to its potential biological and pharmacological activities, [1,1-Biphenyl]-4-ol,4-methoxy-3-methyl-(9CI) is used in research and development for exploring its possible applications in medicine and other fields. Its unique properties make it a valuable tool for scientists and researchers working on innovative solutions and products.
Check Digit Verification of cas no
The CAS Registry Mumber 103594-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,9 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103594-29:
(8*1)+(7*0)+(6*3)+(5*5)+(4*9)+(3*4)+(2*2)+(1*9)=112
112 % 10 = 2
So 103594-29-2 is a valid CAS Registry Number.
103594-29-2Relevant articles and documents
Pd- And Ni-Based Systems for the Catalytic Borylation of Aryl (Pseudo)halides with B2(OH)4
Munteanu, Charissa,Spiller, Taylor E.,Qiu, Jun,Delmonte, Albert J.,Wisniewski, Steven R.,Simmons, Eric M.,Frantz, Doug E.
, p. 10334 - 10349 (2020/09/18)
Despite recent advancements in metal-catalyzed borylations of aryl (pseudo)halides, there is a continuing need to develop robust methods to access both early-stage and late-stage organoboron intermediates amendable for further functionalization. In particular, the development of general catalytic systems that operate under mild reaction conditions across a broad range of electrophilic partners remains elusive. Herein, we report the development and application of three catalytic systems (two Pd-based and one Ni-based) for the direct borylation of aryl (pseudo)halides using tetrahydroxydiboron (B2(OH)4). For the Pd-based catalyst systems, we have identified general reaction conditions that allow for the sequestration of halide ions through simple precipitation that results in catalyst loadings as low as 0.01 mol % (100 ppm) and reaction temperatures as low as room temperature. We also describe a complementary Ni-based catalyst system that employs simple unligated Ni(II) salts as an inexpensive alternative to the Pd-based systems for the borylation of aryl (pseudo)halides. Extrapolation of all three systems to a one-pot tandem borylation/Suzuki-Miyaura cross-coupling is also demonstrated on advanced intermediates and drug substances.
