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[(N,N'-o-phenylenebis(3,5-di-tert-butylsalicylideneimine))Al(Ph3PO)2]Br is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

877242-85-8

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877242-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 877242-85-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,2,4 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 877242-85:
(8*8)+(7*7)+(6*7)+(5*2)+(4*4)+(3*2)+(2*8)+(1*5)=208
208 % 10 = 8
So 877242-85-8 is a valid CAS Registry Number.

877242-85-8Downstream Products

877242-85-8Relevant academic research and scientific papers

Five-coordinate aluminum bromides: Synthesis, structure, cation formation, and cleavage of phosphate ester bonds

Mitra, Amitabha,DePue, Lauren J.,Parkin, Sean,Atwood, David A.

, p. 1147 - 1153 (2006)

The alkane elimination reaction between Salen(tBu)H2 ligands and diethylaluminum bromide was used to prepare three Salen aluminum bromide compounds salen(tBu)AlBr (1) (salen = N,N′-ethylenebis- (3,5-di-tert-butylsalicylideneimine)), salpen(tBu)AlBr (2) (salpen = N,N′-propylenebis(3,5-di-tert-butylsalicylideneimine)), and salophen( tBu)AlBr (3) (salophen = N,N′-o-phenylenenebis(3,5-di-tert- butylsalicylideneimine)). The compounds contain five-coordinate aluminum either in a distorted square pyramidal or a trigonal bipyramidal environment. The bromide group in these compounds could be displaced by triphenylphosphine oxide or triphenyl phosphate to produce the six-coordinate cationic aluminum compounds [salen(tBu)Al(Ph3PO)2]Br (4), [salpen( tBu)Al(Ph3PO)2]Br (5), [salophen( tBu)Al(Ph3PO)2]Br (6), and [salophen-( tBu)Al{(PhO)3PO)}2]Br (7). All the compounds were characterized by 1H, 13C, 27Al, and 31P NMR, IR, mass spectrometry, and melting point. Furthermore, compounds 1-3 and 5-7 were structurally characterized by single-crystal X-ray diffraction. Compounds 1-3 dealkylated a series of organophosphates in stoichiometric reactions by breaking the ester C-O bond. Also, they were catalytic in the dealkylation reaction between trimethyl phosphate and added boron tribromide.

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