860034-11-3 Usage
General Description
4-Bromo-2-nitrophenylboronic acid is a chemical compound that belongs to the class of phenylboronic acids. It is characterized by a bromine atom and a nitro group attached to a phenyl ring, which is in turn connected to a boronic acid group. 4-BROMO-2-NITROPHENYLBORONIC ACID is commonly used as a building block in organic synthesis and medicinal chemistry, particularly in the creation of pharmaceuticals and agrochemicals. Its boronic acid functionality allows it to participate in Suzuki coupling reactions, which are important for the formation of carbon-carbon bonds. Additionally, its nitro and bromo substituents can also be used as directing groups in organic reactions, making 4-bromo-2-nitrophenylboronic acid a versatile and valuable chemical compound for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 860034-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,0,3 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 860034-11:
(8*8)+(7*6)+(6*0)+(5*0)+(4*3)+(3*4)+(2*1)+(1*1)=133
133 % 10 = 3
So 860034-11-3 is a valid CAS Registry Number.
860034-11-3Relevant articles and documents
Novel compound and organic light emitting device comprising the same
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Paragraph 0392; 0401-0403, (2020/05/26)
The present invention provides: a novel compound each comprising an amino group at both ends of a molecule; and an organic light emitting device comprising the same. When the compound of chemical formula 1 of the present invention is applied to the organic light emitting device, it is possible to improve efficiency, lower driving voltage, and improve lifespan characteristics of the organic light emitting device.COPYRIGHT KIPO 2020
A facile and convenient synthesis of functionalized ortho- nitrophenylboronic acids
Collibee, Scott E.,Yu, Jiaxin
, p. 4453 - 4455 (2007/10/03)
A variety of ortho-nitrophenylboronic acids bearing functional groups such as cyano, nitro, halo, α-bromomethyl, and ester were prepared in good yields via I-Mg exchange followed by quenching with trimethyl borate. All reagents employed in this procedure are commercially available and were used without further purification, and the procedure can be executed in about an hour.
