85006-23-1 Usage
Description
3-Aminophenylboronic acid hydrochloride is an organic compound that serves as a versatile intermediate in various chemical reactions and synthesis processes. It is characterized by the presence of an amino group attached to a phenyl ring, with a boronic acid group and a hydrochloride counterion. This unique structure endows it with properties that make it valuable in a range of applications.
Uses
Used in Pharmaceutical Industry:
3-Aminophenylboronic acid hydrochloride is used as a pharmaceutical intermediate for the synthesis of various drugs and medicinal compounds. Its reactivity and functional groups allow for the creation of complex molecules with potential therapeutic effects.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-Aminophenylboronic acid hydrochloride is used as a key building block for the assembly of more complex organic molecules. Its boronic acid moiety is particularly useful in cross-coupling reactions, such as the Suzuki reaction, which facilitates the formation of carbon-carbon bonds.
Used in Research and Development:
3-Aminophenylboronic acid hydrochloride is also utilized in research and development settings, where it can be employed to explore new chemical reactions, develop novel synthetic routes, and investigate the properties of related compounds. Its versatility and reactivity make it a valuable tool for advancing scientific knowledge and innovation in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 85006-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,0 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85006-23:
(7*8)+(6*5)+(5*0)+(4*0)+(3*6)+(2*2)+(1*3)=111
111 % 10 = 1
So 85006-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H8BNO2.ClH/c8-6-3-1-2-5(4-6)7(9)10;/h1-4,9-10H,8H2;1H
85006-23-1Relevant articles and documents
Virtues of Volatility: A Facile Transesterification Approach to Boronic Acids
Hinkes, Stefan P.A.,Klein, Christian D.P.
supporting information, p. 3048 - 3052 (2019/05/10)
Boronic acids are an increasingly important compound class for many applications, including C-C bond formation reactions, medicinal chemistry, and diagnostics. The deprotection of boronic ester intermediates is frequently a problematic and inefficient step in boronic acid syntheses. We describe an approach that highly facilitates this transformation by leveraging the volatility of methylboronic acid and its diol esters. The method is performed under mild conditions, provides high yields, and eliminates cumbersome and problematic purification steps.
