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N-benzyl-3,4-bis(diphenylphosphino)pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119296-22-9

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119296-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119296-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,2,9 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119296-22:
(8*1)+(7*1)+(6*9)+(5*2)+(4*9)+(3*6)+(2*2)+(1*2)=139
139 % 10 = 9
So 119296-22-9 is a valid CAS Registry Number.

119296-22-9Upstream product

119296-22-9Relevant academic research and scientific papers

Process for preparing optically active 1-(p-methoxybenzyl)-1,2,3,4,5,3,7,8-octahydroisoquinoline

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, (2008/06/13)

Optically active 1-(p-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline having the formula (I) is prepared by asymmetric hydrogenation of the corresponding 3,4,5,6,7,8-hexahydro-compound or of the new 1-(p-methoxybenzyl)-3,4,5,6,7,8-hexahydroisoquinoline dihydrogenated phosphate in the present of chiral iridium-phosphine complexes. This product is an intermediate product in the synthesis of cough-relieving dextromethorphanne and analgesic levorphanol. STR1

Optically active 3,4-bis-(diphenylphosphino)-pyrrolidine, and rhodium complexes, containing it as chiral ligands

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, (2008/06/13)

There are described new optically active 3,4-bis-(diphenylphosphino)-pyrrolidines of the formula STR1 wherein Ph is a phenyl group and R is hydrogen, an alkyl group, an arylalkyl group or an acyl group, rhodium complexes containing a compound of formula (I) as its chiral ligands, said rhodium complexes having the formula where (en)2 is two molecules of a monoolefin or one molecule of a diolefin, A is an optically active compound of formula (I) and X- is a tetrafluoroborate, hexafluorophosphate or a perchlorate ion, and use of the rhodium complexes as catalysts for the homogeneous asymmetric hydrogenation of unsubstituted or β-substituted α-acylamino-acrylic acids.

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