90535-47-0 Usage
Description
(3-phenoxypropyl)boronic acid is a versatile boronic acid derivative characterized by its unique structure, consisting of a boron atom attached to a (3-phenoxypropyl) group. It is commonly used in organic chemistry as a building block for the preparation of various pharmaceuticals, agrochemicals, and materials.
Uses
Used in Organic Synthesis:
(3-phenoxypropyl)boronic acid is used as a reagent or catalyst in organic synthesis reactions, such as Suzuki-Miyaura cross-coupling reactions, for the formation of carbon-carbon bonds. Its reactivity and selectivity make it a valuable tool in the construction of complex organic molecules.
Used in Medicinal Chemistry:
(3-phenoxypropyl)boronic acid is used as a building block in the development of pharmaceuticals due to its ability to form strong and selective interactions with biological targets.
Used in Material Science:
(3-phenoxypropyl)boronic acid is used in the development of new materials due to its ability to form strong and selective interactions with specific functional groups in materials.
Check Digit Verification of cas no
The CAS Registry Mumber 90535-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,3 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90535-47:
(7*9)+(6*0)+(5*5)+(4*3)+(3*5)+(2*4)+(1*7)=130
130 % 10 = 0
So 90535-47-0 is a valid CAS Registry Number.
90535-47-0Relevant articles and documents
Coupling of Trifluoroacetaldehyde N-Triftosylhydrazone with Organoboronic Acids for the Synthesis of gem-Difluoroalkenes
Ma, Yu,Reddy, Bhoomireddy Rajendra Prasad,Bi, Xihe
supporting information, p. 9860 - 9863 (2019/12/24)
The synthesis of alkyl gem-difluoroalkenes remains a difficult task in organic synthesis. Here, we report a general and efficient approach for tackling this problem by gem-difluoroolefination of trifluoroacetaldehyde N-triftosylhydrazone with organoboronic acids. This protocol is operationally simple, free of transition metals, and suitable for a broad range of organoboronic acids. Moreover, the utility of the products was demonstrated by further conversion of the gem-difluorovinyl group.
Copper-promoted trifluoromethylation of primary and secondary alkylboronic acids
Xu, Jun,Xiao, Bin,Xie, Chuan-Qi,Luo, Dong-Fen,Liu, Lei,Fu, Yao
, p. 12551 - 12554 (2013/02/22)
New couple: The Cu-promoted trifluoromethylation of primary and secondary alkylboronic acids with TMSCF3 extends the scope of transition-metal-catalyzed trifluoromethylation reactions to sp 3-hybridized carbon centers. It also repres
