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2-(2-nitro-phenyl)-benzo[1,3,2]dioxaborole is a complex organic compound with the molecular formula C13H8BNO4. It is a derivative of benzo[1,3,2]dioxaborole, featuring a nitro group attached to the phenyl ring. 2-(2-nitro-phenyl)-benzo[1,3,2]dioxaborole is known for its reactivity and is often used in organic synthesis, particularly in cross-coupling reactions. It serves as a valuable intermediate in the formation of various pharmaceuticals and other complex organic molecules. The nitro group in 2-(2-nitro-phenyl)-benzo[1,3,2]dioxaborole can be reduced to an amine group, which is a common transformation in the synthesis of nitrogen-containing compounds. Its stability and reactivity make it a useful building block in the development of new chemical entities.

5785-84-2

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5785-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5785-84-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5785-84:
(6*5)+(5*7)+(4*8)+(3*5)+(2*8)+(1*4)=132
132 % 10 = 2
So 5785-84-2 is a valid CAS Registry Number.

5785-84-2Downstream Products

5785-84-2Relevant 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

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