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(S)-N-benzyl-1-(1-naphthyl)-3-butenylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1374646-03-3

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1374646-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374646-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,6,4 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1374646-03:
(9*1)+(8*3)+(7*7)+(6*4)+(5*6)+(4*4)+(3*6)+(2*0)+(1*3)=173
173 % 10 = 3
So 1374646-03-3 is a valid CAS Registry Number.

1374646-03-3Downstream Products

1374646-03-3Relevant academic research and scientific papers

Menthane-Based Chloride-Bridged η3-Bis-π-Allylpalladium Chloride Dimers: Catalytic Asymmetric Allylation of Imines

Jha, Amit K.,Fernandes, Rodney A.

, p. 2857 - 2863 (2019/05/15)

Menthane-based η3-bis-π-allylpalladium chloride dimer complexes have been prepared for the first time. They exist as dimeric η3-bis-π-allylpalladium with four chloride bridges. The complexes catalyze the asymmetric allylation of vari

Development of the first menthane-based chiral bis(π-allylpalladium) catalysis: Asymmetric allylation of imines

Fernandes, Rodney A.,Chaudhari, Dipali A.

experimental part, p. 1945 - 1952 (2012/05/20)

A new ethylidene menthane-based chiral π-allylpalladium complex catalyzes the asymmetric allylation of various imines with allyltributylstannane and 1 equiv. of water to give chiral homoallylamines in good yields and enantioselectivities. The reaction was carried out essentially under neutral conditions and displayed a good transfer of chiral information from the menthane skeleton through the formation of a bis(π-allylpalladium) species. This is the first example of menthane-based chiral bis(π-allylpalladium) catalysis. A menthane-based chiral π-allylpalladium-catalyzed asymmetric allylation of various imines has been developed giving chiral homoallylamines in good yields and enantioselectivities. The reaction displays a good transfer of chiral information from the menthane skeleton through the formation of a bis(π-allylpalladium) complex. Copyright

Enantioselective allylation of imines catalyzed by newly developed (-)-β-pinene-based π-allylpalladium catalyst: An efficient synthesis of (R)-α-propylpiperonylamine and (R)-pipecolic acid

Fernandes, Rodney A.,Nallasivam, Jothi L.

, p. 7789 - 7800 (2013/04/23)

A newly developed π-allylpalladium with a (-)-β-pinene framework and an isobutyl side chain catalyzed the enantioselective allylation of imines in good yields and enantioselectivities (20 examples, up to 98% ee). An efficient enantioselective synthesis of the (R)-α-propyl piperonylamine part of DMP 777, a human leukocyte elastase inhibitor and (R)-pipecolic acid have been achieved as a useful application of this methodology. The Royal Society of Chemistry 2012.

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