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30504-61-1

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30504-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30504-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,0 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30504-61:
(7*3)+(6*0)+(5*5)+(4*0)+(3*4)+(2*6)+(1*1)=71
71 % 10 = 1
So 30504-61-1 is a valid CAS Registry Number.

30504-61-1Relevant articles and documents

BTK Inhibitors and uses thereof

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Paragraph 0574-0580, (2020/05/02)

The invention discloses a bruton's tyrosine kinase (BTK) inhibitor and use thereof. Specifically, the invention provides heteroaromatic compounds or stereoisomers, geometrical isomers, tautomers, racemates, nitrogen oxides, hydrates, solvates, metabolites and pharmaceutically acceptable salts or prodrugs thereof, and pharmaceutical compositions containing the heteroaromatic compounds; the invention also discloses use of the heteroaromatic compounds or the pharmaceutical compositions containing the heteroaromatic compounds in preparation of medicines; the medicines can be used for treating autoimmune diseases, inflammatory diseases or proliferative diseases.

Gold nanoparticles supported on TiO2 catalyse the cycloisomerisation/oxidative dimerisation of aryl propargyl ethers

Efe, Christina,Lykakis, Ioannis N.,Stratakis, Manolis

supporting information; experimental part, p. 803 - 805 (2011/04/12)

Gold nanoparticles supported on TiO2 (~1%) catalyse in high yields the selective cycloisomerisation of aryl propargyl ethers into the corresponding 2H-chromenes, under heterogeneous conditions. 2H,2′H-3, 3′-Bichromenes resulting from a catalytic oxidative dimerization pathway are also formed as by-products. The Royal Society of Chemistry 2011.

Copper(I) iodide: A catalyst for the improved synthesis of aryl propargyl ethers

Bell,Davies,Geen,Mann

, p. 707 - 712 (2007/10/02)

Copper(I) iodide catalyses the reaction between phenols and dialkylpropargyl chlorides to give aryl 1,1-dialkylpropargyl ethers 5 a-k and 7a-e in good yields and purity. These ethers are important as precursors to the 2H-1-benzopyrans 8a-l and 9a-e.

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