908142-03-0 Usage
Uses
Used in Suzuki Reaction:
(3-(hydroxyMethyl)-4-Methoxyphenyl)boronic acid is used as a reactant in the Suzuki reaction, a widely employed cross-coupling process in organic synthesis. This reaction facilitates the formation of carbon-carbon bonds between an aryl or vinyl boronic acid and an organic halide or triflate, leading to the synthesis of biaryl compounds. The use of this boronic acid in the Suzuki reaction allows for the creation of new molecular structures with potential applications in various fields.
Used in Organic Synthesis:
(3-(hydroxyMethyl)-4-Methoxyphenyl)boronic acid is used as an intermediate in organic synthesis for the development of complex organic molecules. Its unique functional groups and reactivity make it a valuable building block for the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
(3-(hydroxyMethyl)-4-Methoxyphenyl)boronic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence in the molecular structure can impart specific biological activities, making it a valuable component in the development of new drugs and therapeutic agents. The hydroxymethyl and methoxy substituents on the phenyl ring can influence the pharmacokinetic and pharmacodynamic properties of the resulting drug molecules, potentially leading to improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 908142-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,1,4 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 908142-03:
(8*9)+(7*0)+(6*8)+(5*1)+(4*4)+(3*2)+(2*0)+(1*3)=150
150 % 10 = 0
So 908142-03-0 is a valid CAS Registry Number.
908142-03-0Relevant articles and documents
COMPOUND, RESIN PRECURSOR, CURED PRODUCT, OPTICAL ELEMENT, OPTICAL SYSTEM, INTERCHANGEABLE LENS FOR CAMERA, OPTICAL DEVICE, CEMENTED LENS, AND PRODUCTION METHOD FOR CEMENTED LENS
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Paragraph 0113-0115, (2020/08/12)
A compound expressed in the following formula (1) (where R1 and R2 independently denote a hydrogen atom or a methyl group, Y1 and Y2 independently denote an alkylene group having a carbon number of 1 to 9, and n1 and n2 independently denote an integer of 0 to 3).
New insights into the SAR and binding modes of bis(hydroxyphenyl)thiophenes and -benzenes: Influence of additional substituents on 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) inhibitory activity and selectivity
Bey, Emmanuel,Marchais-Oberwinkler, Sandrine,Negri, Matthias,Kruchten, Patricia,Oster, Alexander,Klein, Tobias,Spadaro, Alessandro,Werth, Ruth,Frotscher, Martin,Birk, Barbara,Hartmann, Rolf W.
scheme or table, p. 6724 - 6743 (2010/04/05)
17β-Hydroxysteroid dehydrogenase type 1 (17β-HSD1) is responsible for the catalytic reduction of weakly active E1 to highly potent E2. E2 stimulates the proliferation of hormone-dependent diseases via activation of the estrogen receptor α (ERα). Because o
