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(S)-2-(2,3-bis(diisopropylamino)cycloallylamino)-3-phenylpropan-1-ol hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1366421-75-1

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1366421-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1366421-75-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,6,4,2 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1366421-75:
(9*1)+(8*3)+(7*6)+(6*6)+(5*4)+(4*2)+(3*1)+(2*7)+(1*5)=161
161 % 10 = 1
So 1366421-75-1 is a valid CAS Registry Number.

1366421-75-1Relevant academic research and scientific papers

CYCLOPROPENIMINE CATALYST COMPOSITIONS AND PROCESSES

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Paragraph 0201; 0202, (2013/05/09)

The present invention provides, inter alia, a cyclopropenimine Br?nsted base catalyst and a cyclopropenimine scaffold for use as a Br?nsted base catalyst. This cyclopropenimine has the structure (100). Methods for making such a cyclopropenimine are also provided. Further provided are processes for carrying out an organic synthetic reaction and processes for catalyzing a proton transfer reaction enantioselectively using such a cyclopropenimine Br?nsted base catalyst.

Enantioselective Bronsted base catalysis with chiral cyclopropenimines

Bandar, Jeffrey S.,Lambert, Tristan H.

supporting information; experimental part, p. 5552 - 5555 (2012/05/20)

Cyclopropenimines are shown to be a highly effective new class of enantioselective Bronsted base catalysts. A chiral 2,3-bis(dialkylamino) cyclopropenimine catalyzes the rapid Michael reaction of a glycine imine substrate with high levels of enantioselectivity. A preparative scale reaction to deliver 25 g of product is demonstrated, and a trivial large scale synthesis of the optimal catalyst is shown. In addition, the basicity of a 2,3-bis(dialkylamino)cyclopropenimine is measured for the first time and shown to be approximately equivalent to the P1-tBu phosphazene base. An X-ray crystal structure of the protonated catalyst is shown along with a proposed mechanistic and stereochemical rationale.

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