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84299-18-3

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84299-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84299-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,9 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84299-18:
(7*8)+(6*4)+(5*2)+(4*9)+(3*9)+(2*1)+(1*8)=163
163 % 10 = 3
So 84299-18-3 is a valid CAS Registry Number.

84299-18-3Relevant articles and documents

Chiral integrated catalysts composed of bifunctional thiourea and arylboronic acid: Asymmetric aza-Michael addition of α,β-unsaturated carboxylic acids

Hayama, Noboru,Azuma, Takumi,Kobayashi, Yusuke,Takemoto, Yoshiji

, p. 704 - 717 (2016)

The first intermolecular asymmetric Michael addition of nitrogen-nucleophiles to α,β-unsaturated carboxylic acids was achieved through a new type of arylboronic acid equipped with chiral aminothiourea. The use of BnONH2 as a nucleophile gives a range of enantioenriched β-(benzyloxy)amino acid derivatives in good yields and with high enantioselectivity (up to 90% yield, 97% enantiomeric excess (ee)). The obtained products are efficiently converted to optically active β-amino acid and 1,2-diamine derivatives.

Tungsten(0) alkylidene complexes stabilized as pyridinium ylides: New aspects of their synthesis and reactivity

Rudler, Henri,Durand-Réville, Thomas

, p. 571 - 587 (2007/10/03)

The interaction of dihydropyridines with alkoxycarbene complexes of tungsten has been shown to lead to pyridinium ylid complexes: this transformation has now been applied to the synthesis of a hydroxyl-containing ylid complex by ring-opening of the pentacarbonyl (2-oxacyclopentylidene) tungsten(0) complex and to the synthesis of a series of chiral ylid complexes both from chiral and non-chiral carbene complexes by the use of dihydropyridines and dihydronicotines, respectively. The transfer of the alkylidene moiety of these complexes to nucleophilic olefins will be outlined and discussed. Especially relevant is the interaction of these pyridinium ylid complexes with unsaturated substrates such as dihydropyridines, enamines, and β-alkoxy bis(trimethyl-silyl) ketene acetals. This latter reaction leads to conjugated carboxylic acids, and has been be applied to a new synthesis of a honey bee pheromone, the queen substance.

Dual inhibition of phosphodiesterase 4 and matrix metalloproteinases by an (arylsulfonyl)hydroxamic acid template [3]

Groneberg, Robert D.,Burns, Christopher J.,Morrissette, Matthew M.,Ullrich, John W.,Morris, Robert L.,Darnbrough, Shelley,Djuric, Stevan W.,Condon, Stephen M.,McGeehan, Gerard M.,Labaudiniere, Richard,Neuenschwander, Kent,Scotese, Anthony C.,Kline, Jane A.

, p. 541 - 544 (2007/10/03)

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