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100244-17-5

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100244-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100244-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,4 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100244-17:
(8*1)+(7*0)+(6*0)+(5*2)+(4*4)+(3*4)+(2*1)+(1*7)=55
55 % 10 = 5
So 100244-17-5 is a valid CAS Registry Number.

100244-17-5Relevant academic research and scientific papers

Novel synthesis of chiral 1,3-diphosphines via palladium template promoted hydrophosphination and functional group transformation reactions

Yuan, Mingjun,Pullarkat, Sumod A.,Li, Yongxin,Lee, Zhi-Yi,Leung, Pak-Hing

, p. 3582 - 3588 (2010)

A novel cyano-functionalized monophosphine palladium substrate containing the ortho-metalated (R)-(1-(dimethylamino)ethyl)naphthalene as the chiral auxiliary was synthesized from 3-chloropropionaldehyde diethylacetal via a one-pot process. The asymmetric hydrophosphination reactions between diphenylphosphine and the trans-or cis-monophosphine substrates were carried out under mild conditions, which gave the corresponding cyano-substituted chiral 1,3-bis(diphenylphosphino)propane palladium complexes with good yields and stereoselectivities. Subsequent functional group transformation reactions were conducted by successive treatment of the hydrophosphination products with Dibal-H and chemoselectively yielded the formyl-and hydroxyl-functionalized chiral 1,3-diphosphine complexes. The absolute configurations and coordination information of the novel 1,3-diphosphine complexes were analyzed by X-ray crystallography. The optically pure 1,3-bis(diphenylphosphino)propane ligands with cyano, formyl, and hydroxyl functionalities could be liberated in high yields from the corresponding dihalo palladium complexes by treatment with aqueous potassium cyanide.

New cyclic phosphonium salts derived from the reaction of phosphine-aldehydes with acid

Mikhailine, Alexandre A.,Lagaditis, Paraskevi O.,Sues, Peter E.,Lough, Alan J.,Morris, Robert H.

scheme or table, p. 1824 - 1830 (2010/08/06)

Various cyclic phosphonium structures are formed in high yield by the deprotection of unstable phosphine-aldehydes in acidic solution. When there is a methylene spacer between the phosphine and the aldehyde, a phosphonium ion [PHR2CH2CH(OEt)2]Br2, R=iPrOH, Et is obtained. Reaction of these phosphonium salts with water produces the dimers [-PR2CH2CH(OH)-]2[Br]2?R = iPr, Et. When there is an ethylene spacer as in PPh2CH2CH2CH(OCH2CH2O), a remarkable tetramer with a 16-membered ring [-PPh2CH2CH2CH (OH)-]4[Cl]4 forms as one diastereomer in hydrochloric acid solution. Reaction of HCl with the protected phosphine-aldehyde with a propylene spacer (PPh2CH2CH2CH2CH(OCH2CH2O)) results in the formation of the monomeric phosphonium salt [-PPh2 CH2CH2CH2CH(OH)-]Cl with a 5-membered ring. Solid state structures of different ring types were determined using X-ray diffraction experiment.

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