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(3R,4S)-4-((R)-1-Hydroxy-but-3-ynyl)-3-methoxy-1-(4-methoxy-phenyl)-azetidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

444083-12-9

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444083-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 444083-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,0,8 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 444083-12:
(8*4)+(7*4)+(6*4)+(5*0)+(4*8)+(3*3)+(2*1)+(1*2)=129
129 % 10 = 9
So 444083-12-9 is a valid CAS Registry Number.

444083-12-9Relevant academic research and scientific papers

Additions of allenyl/propargyl organometallic reagents to 4-oxoazetidine-2-carbaldehydes: Novel palladium-catalyzed domino reactions in allenynes

Alcaide, Benito,Almendros, Pedro,Aragoncillo, Cristina

, p. 1719 - 1729 (2002)

Metal-mediated carbonyl allenylation and propargylation of 4-oxoazetidine-2-carbaldehydes were investigated in aqueous environment. Different propargyl bromide and metal promoters showed varied regio- and stereoselectivities on product formation. In addit

Metal-catalyzed cycloisomerization and tandem oxycyclization/hydroxylation of alkynols: Synthesis of nonfused, spiranic and fused oxabicyclic β-lactams

Alcaide, Benito,Almendros, Pedro,Del Campo, Teresa Martinez,Carrascosa, Rocio

scheme or table, p. 4912 - 4919 (2010/10/19)

2-Azetidinone-tethered alkynols, readily prepared from the corresponding aldehydes or ketones, were used as starting materials for the oxycyclization reaction catalyzed by precious metals. AgOAc exclusively affords dihydrofurans, methylenetetrahydrofurans, or methylenetetrahydro-2H-pyrans through specific 5-endo, 5-exo, or 6-exo pathways, respectively. Interestingly, in the presence of a catalytic amount: of PtII or AuIII salts, cyclization reactions occurred preferentially through a tandem oxycyclization/hydroxylation of alkynols to afford a variety of nonfused, spiranic and fused oxabicyclic β-lactams in moderate to high yields. Besides, it has been observed that the tandem gold-catalyzed cycloetherification/hydroxylation of a methoxymethyl alkynyl ether can be accomplished.

New aspects of the indium chemistry of carbonyl-β-lactams

Alcaide, Benito,Almendros, Pedro,Aragoncillo, Cristina,Rodri?guez-Acebes, Raquel

, p. 1163 - 1170 (2007/10/03)

Reactions of racemic as well as optically pure carbonyl-β-lactams with stabilized organo-indium reagents were investigated in aqueous media. The regio- and stereochemistry of the processes were generally good, offering a convenient asymmetric entry to den

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