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1476048-33-5

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1476048-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1476048-33-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,7,6,0,4 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1476048-33:
(9*1)+(8*4)+(7*7)+(6*6)+(5*0)+(4*4)+(3*8)+(2*3)+(1*3)=175
175 % 10 = 5
So 1476048-33-5 is a valid CAS Registry Number.

1476048-33-5Downstream Products

1476048-33-5Relevant academic research and scientific papers

Design and synthesis of angularly annulated spirocyclics via enyne metathesis and the Diels-Alder reaction as key steps

Kotha, Sambasivarao,Ali, Rashid,Tiwari, Arti

, p. 2471 - 2480 (2014)

We have developed a simple and an efficient route to a range of angularly fused spirocycles by the application of enyne metathesis and the Diels-Alder reaction as key steps. The enyne metathesis protocol has been further extended to the dibenzylation of indane-1,3-dione by using cross-enyne metathesis in the presence of hexa-1,5-diene with the aid of Grubbs' 1st generation catalyst followed by an aromatization sequence with DDQ. Georg Thieme Verlag Stuttgart New York.

Design and Synthesis of Angularly Annulated Spirocyclics via Enyne Metathesis and the Diels-Alder Reaction as Key Steps

Kotha, Sambasivarao,Ali, Rashid,Tiwari, Arti

, p. 2471 - 2480 (2015/12/26)

We have developed a simple and an efficient route to a range of angularly fused spirocycles by the application of enyne metathesis and the Diels-Alder reaction as key steps. The enyne metathesis protocol has been further extended to the dibenzylation of indane-1,3-dione by using cross-enyne metathesis in the presence of hexa-1,5-diene with the aid of Grubbs' 1st generation catalyst followed by an aromatization sequence with DDQ.

Diversity-oriented approach to novel spirocyclics via enyne metathesis, diels-alder reaction, and a [2+2+2] cycloaddition as key steps

Kotha, Sambasivarao,Ali, Rashid,Tiwari, Arti

, p. 1921 - 1926 (2013/09/24)

A simple protocol for the synthesis of indane-based spirocyclics has been developed via enyne metathesis, Diels-Alder reaction, and a [2+2+2] cycloaddition as key steps starting from indane-1,3-dione. The key diene building block was assembled by enyne metathesis. In this sequence, rongalite is used as a green reagent to prepare the sultine intermediate, which is a useful precursor to generate the transient diene.

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