105365-51-3 Usage
Description
4-Butoxyphenylboronic Acid is an organic compound that contains a boron atom bonded to a phenyl group with a butoxy substituent. It is a versatile reagent in organic synthesis and has various applications in different industries.
Uses
Used in Chemical Synthesis:
4-Butoxyphenylboronic Acid is used as a reactant for Suzuki-Miyaura cross-coupling reactions, which are widely used in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials.
Used in Condensation Reactions:
4-Butoxyphenylboronic Acid is used as a reactant in condensation reactions, which are important for the formation of complex organic molecules and the synthesis of natural products.
Used in Synthesis of Azobenzene-Functionalized Compounds:
4-Butoxyphenylboronic Acid is used as a reactant for the synthesis of azobenzene-functionalized compounds, which have potential applications in the development of smart materials and molecular switches.
Used in Preparation of Highly Fluorescent Diketopyrrolopyrrole Derivatives:
4-Butoxyphenylboronic Acid is used as a reactant for the preparation of highly fluorescent diketopyrrolopyrrole derivatives, which have potential applications in the fields of bioimaging, sensing, and optoelectronics.
Used in Rhodium-Catalyzed Suzuki-Type Cross-Coupling:
4-Butoxyphenylboronic Acid is used as a reactant in rhodium-catalyzed Suzuki-type cross-coupling reactions, which are useful for the synthesis of various organic compounds, including heterocycles and natural products.
Used in Copper-Catalyzed Asymmetric Conjugate Reduction of Coumarins:
4-Butoxyphenylboronic Acid is used as a reactant in copper-catalyzed asymmetric conjugate reduction of coumarins, which is an important reaction for the synthesis of enantioenriched compounds with potential applications in pharmaceuticals and agrochemicals.
General Description:
4-Butoxyphenylboronic Acid contains varying amounts of anhydride, which may affect its reactivity and applications in different chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 105365-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,6 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105365-51:
(8*1)+(7*0)+(6*5)+(5*3)+(4*6)+(3*5)+(2*5)+(1*1)=103
103 % 10 = 3
So 105365-51-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H15BO3/c1-2-3-8-14-10-6-4-9(5-7-10)11(12)13/h4-7,12-13H,2-3,8H2,1H3
105365-51-3Relevant articles and documents
Design and synthesis of a new family of fluorinated liquid crystals
Nenajdenko, Valentine G.,Goldberg, Aleksey A.,Muzalevskiy, Vasily M.,Balenkova, Elizabeth S.,Shastin, Aleksey V.
supporting information, p. 2370 - 2383 (2013/03/28)
A convenient and simple three-step pathway to the new family of CF 2CF2S-bridged alkanes and CF2S-, CF 2O-bridged alkenes and alkynes was elaborated by using catalytic olefination reaction as a key step of the s
