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N-Butyliden-tert-butylamine is an organic compound with the chemical formula C8H17N. It is a colorless liquid with a strong, pungent odor and is soluble in water. This amine is formed by the condensation of butyraldehyde with tert-butylamine, and it is used as an intermediate in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is important to handle N-butyliden-tert-butylamine with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

6852-59-1

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6852-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6852-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6852-59:
(6*6)+(5*8)+(4*5)+(3*2)+(2*5)+(1*9)=121
121 % 10 = 1
So 6852-59-1 is a valid CAS Registry Number.

6852-59-1Relevant academic research and scientific papers

Catalytic hydrogenation with frustrated lewis pairs: Selectivity achieved by size-exclusion design of lewis acids

Eroes, Gabor,Nagy, Krisztina,Mehdi, Hasan,Papai, Imre,Nagy, Peter,Kiraly, Peter,Tarkanyi, Gabor,Soos, Tibor

scheme or table, p. 574 - 585 (2012/03/08)

Catalytic hydrogenation that utilizes frustrated Lewis pair (FLP) catalysts is a subject of growing interest because such catalysts offer a unique opportunity for the development of transition-metal-free hydrogenations. The aim of our recent efforts is to further increase the functional-group tolerance and chemoselectivity of FLP catalysts by means of size-exclusion catalyst design. Given that hydrogen molecule is the smallest molecule, our modified Lewis acids feature a highly shielded boron center that still allows the cleavage of the hydrogen but avoids undesirable FLP reactivity by simple physical constraint. As a result, greater latitude in substrate scope can be achieved, as exemplified by the chemoselective reduction of α,β-unsaturated imines, ketones, and quinolines. In addition to synthetic aspects, detailed NMR spectroscopic, DFT, and 2H isotopic labeling studies were performed to gain further mechanistic insight into FLP hydrogenation. Copyright

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