85107-44-4 Usage
Molecular structure
2-(3-nitro-phenyl)-[1,3,2]dioxaborinane consists of a boron atom bonded to two oxygen atoms and a phenyl ring with a nitro group attached.
Type of compound
It is a chemical compound commonly used in organic synthesis.
Reactivity
2-(3-nitro-phenyl)-[1,3,2]dioxaborinane is highly reactive and is often used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds.
Applications
It is commonly employed in Suzuki-Miyaura cross-coupling reactions for the construction of biaryl compounds and has been utilized in the pharmaceutical industry for the synthesis of various drug molecules.
Importance
Its unique structure and reactivity make 2-(3-nitro-phenyl)-[1,3,2]dioxaborinane an important building block in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 85107-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,0 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85107-44:
(7*8)+(6*5)+(5*1)+(4*0)+(3*7)+(2*4)+(1*4)=124
124 % 10 = 4
So 85107-44-4 is a valid CAS Registry Number.
85107-44-4Relevant academic research and scientific papers
Derivatization and Mass Spectrometric Investigation of Substituted Benzeneboronic Acids. The Use of Linked Scanning During Gas Chromatography Mass Spectrometry
Longstaff, Colin,Rose, Malcolm Edward
, p. 508 - 518 (2007/10/02)
Substituted benzeneboronic acids are important intermediates in the synthesis of support matrices for affinity chromatography but their analysis by mass spectrometry is hindered by thermal reactions in the ion source.A simple derivatization with 1,2- or 1
