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93144-85-5

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93144-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93144-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,4 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93144-85:
(7*9)+(6*3)+(5*1)+(4*4)+(3*4)+(2*8)+(1*5)=135
135 % 10 = 5
So 93144-85-5 is a valid CAS Registry Number.

93144-85-5Downstream Products

93144-85-5Relevant academic research and scientific papers

Metal-free diastereoselective catalytic hydrogenations of imines using B(C6F5)3

Heiden, Zachariah M.,Stephan, Douglas W.

, p. 5729 - 5731 (2011/07/08)

Reductions of chiral ketimines effected under H2 by catalytic amounts of B(C6F5)3 result in moderate to excellent diastereoselectivities. In the case of camphor and menthone derived imines, the reductions procee

Reductive Aminations of Ketones and Aldehydes using Borane-Pyridine

Pelter, Andrew,Rosser, Richard M.,Mills, Stuart

, p. 717 - 720 (2007/10/02)

Borane-pyridine is introduced as a cheap and readily available alternative to sodium cyanotrihydroborate for the purpose of the reductive amination of a wide variety of carbonyl compounds.It does not suffer from the severe toxicity associated with sodium cyanotrihydroborate.

Amines as Dehalogenating Agents. IV. Hydrocarbons, N-Bornyl- and N-Isobornylaniline Formation in the Reaction between 3-Bromocamphor and N-Methylaniline

Giumanini, Angelo G.,Musiani, Marco M.

, p. 423 - 428 (2007/10/02)

N-Methylanilin (4) reagiert bei 200 deg C im Vergleich zu N,N-Dimethylanilin entweder mit 3-Bromcamphor (2) oder Camphor (3) zu den Kohlenwasserstoffen, Camphen 5 und Tricyclen 6 und N-Bornylanilin (exo-endo-Isomers 7).Bei der Reaktion mit 3 ist Saeurekatalyse notwenig.Untersuchungen zum Mechanismus erlauben es, anzunehmen, dass Camphoranil 8 ein gemeinsames Zwischenprodukt fuer alle Produkte und 4 der H-Donator in den Reduktionsstufen ist, auf der Grundlage von kinetischen und stereochemischen Beweisen und unabhaengigen chemischen Experimenten.

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