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1H-Tetrazaborole, 4,5-dihydro-1,5-bis(1-methylpropyl)-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90756-22-2

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90756-22-2 Usage

Type of compound

Boron-containing heterocyclic compound

Usage

Various organic and medicinal chemistry applications

Potential pharmacological properties

Studied for potential use in treatment of various medical conditions, including cancer and neurological disorders

Use as building block

In the synthesis of pharmaceuticals and other biologically active compounds

Unique structure and properties

Valuable tool in chemical research and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 90756-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,5 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90756-22:
(7*9)+(6*0)+(5*7)+(4*5)+(3*6)+(2*2)+(1*2)=142
142 % 10 = 2
So 90756-22-2 is a valid CAS Registry Number.

90756-22-2Downstream Products

90756-22-2Relevant academic research and scientific papers

Iminoboranes from the Thermal Decomposition of Dialkylazidoboranes

Meier, Hans-Ulrich,Paetzold, Peter,Schroeder, Ernst

, p. 1954 - 1964 (2007/10/02)

Iminoboranes RB = NR (1a - f) are formed by the thermal decomposition of azidoboranes R2BN3 (5a - f) in the gas phase or in solution.At low temperature, the iminoboranes 1b, d, e (R = iPr, iBu, sBu) can be trapped from the gas phase.They are characterized and brought to reaction as isolated species.Without other reactands, the iminoboranes dimerize or trimerize to form the cyclic products 2 or 3, respectively, or polymerize to the wax-like solids 4.Produced in solution below 100 deg C, the iminoboranes are azidoborated by the educts 5 to give the (azidoboryl)amines 6 which are transformed into the borazines 3 at 160 - 180 deg C.Iminoborazines undergo an ethyloboration with BEt3, a cycloaddition with PhN3, and in the absence of the strongly reactive R2BN3 a concurring cycloaddition and azidosilation with Me3SiN3 with formation of 7 - 10, respectively.

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