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153255-45-9

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153255-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153255-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,2,5 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153255-45:
(8*1)+(7*5)+(6*3)+(5*2)+(4*5)+(3*5)+(2*4)+(1*5)=119
119 % 10 = 9
So 153255-45-9 is a valid CAS Registry Number.

153255-45-9Downstream Products

153255-45-9Relevant academic research and scientific papers

Reactions of β-diketiminate-stabilized calcium amides with 9-borabicyclo[3.3.1]nonane (9-BBN)

Barrett, Anthony G.M.,Crimmin, Mark R.,Hill, Michael S.,Hitchcock, Peter B.,Procopiou, Panayiotis A.

, p. 4076 - 4079 (2007)

The reaction of a β-diketiminate-stabilized calcium diphenylamide with the dialkylborane 9-BBN allows the synthesis of a β-diketiminate- stabilized calcium borohydride along with an amidoborane reaction coproduct via a likely σ-bond metathesis mechanism.

Reactions of titanium hydrazides with silanes and boranes: N-N bond cleavage and N atom functionalization

Stevenson, Laura C.,Mellino, Simona,Clot, Eric,Mountford, Philip

, p. 10140 - 10143 (2015)

Reaction of Ti(N2iPrN)(NNPh2)(py) with Ph(R)SiH2 (R = H, Ph) or 9-BBN gave reductive cleavage of the Nα-Nβ bond and formation of new silyl- or boryl-amido ligands. The corresponding reactions of CpTi{MeC(NiPr)2}(NNR2) (R = Me or Ph) with HBPin or 9-BBN gave borylhydrazido-hydride or borylimido products, respectively. Nα and Nβ atom transfer and dehydrogenative coupling reactions are also reported.

Alkaline-Earth-Catalyzed Dehydrocoupling of Amines and Boranes

Liptrot, David J.,Hill, Michael S.,Mahon, Mary F.,Wilson, Andrew S. S.

supporting information, p. 13362 - 13365 (2015/11/09)

Dehydrocoupling reactions between the boranes HBpin and 9-borabicyclo[3.3.1]nonane and a range of amines and anilines ensue under very mild reaction conditions in the presence of a simple β-diketiminato magnesium n-butyl precatalyst. The facility of the reactions is suggested to be a function of the Lewis acidity of the borane substrate, and is dictated by resultant pre-equilibria between, and the relative stability of, magnesium hydride and borohydride intermediates during the course of the catalysis.

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