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4-formyldodecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73401-51-1

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73401-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73401-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,0 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73401-51:
(7*7)+(6*3)+(5*4)+(4*0)+(3*1)+(2*5)+(1*1)=101
101 % 10 = 1
So 73401-51-1 is a valid CAS Registry Number.

73401-51-1Downstream Products

73401-51-1Relevant academic research and scientific papers

COMPARATIVE STUDY OF TRIPHENYLAMINE, TRIPHENYLPHOSPHINE, TRIPHENYLARSINE, TRIPHENYLANTIMONY AND TRIPHENYLBISMUTH AS LIGANDS IN THE RHODIUM-CATALYZED HYDROFORMYLATION OF 1-DODECENE

Carlock, John T.

, p. 185 - 188 (1984)

Triphenylamine, triphenylphosphine, triphenylarsine, triphenylantimony and triphenylbismuth were evaluated on the basis of olefin to aldehyde converion, and also on the basis of the normal/iso (n/i) product ratio, as ligands in the rhodium-catalyzed hydroformylation of 1-dodecene.Two series of reactions were conducted which differed only in total reaction time (120 minutes vs 135 minutes) and in the ligand/rhodium ratio (60:1 vs 300:1).Both reactions series employed 35 grams of 1-dodecene, a 176 ppm rhodium charge, 100 psig of 1:1 H2/CO, and a reaction temperature of 90 deg C.In the 60:1 vs 330:1 reaction series, triphenylamine gave olefin conversion and n/i ratios of 2.0 percent, 2.0 vs 5.8 percent, 1.8; triphenylphosphine gave 95 percent, 4.4 vs 86.9 percent, 8.7; triphenylarsine gave 58 percent, 3.1 vs 85.8 percent, 3.5; triphenylantimony gave13.0 percent, 6.1 vs 3.5 percent, 9.1 respectively.Triphenylbismuth failed to promote hydroformylation in both reaction series.These data demonstrate that regiospecificity, as measured by the n/i product ratio, varies inversly to increased ligand basicity.

Aldehydes substituted in alpha position by alkyl residues as odoriferous and aroma substances

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Page/Page column 10-11, (2010/11/29)

The present invention primarily relates to the use of an aldehyde, substituted in alpha position by an alkyl residue, of the formula having (I) a total of 13 C atoms, wherein R means an unbranched alkyl residue having 6, 7, 8 or 9 C atomsandR′ means an unbranched alkyl residue having 2, 3, 4 or 5 C atoms, or (II) a total of 15 C atoms, wherein R means an unbranched alkyl residue having 8, 9, 10 or 11 C atomsandR′ means an unbranched alkyl residue having 2, 3, 4 or 5 C atoms,or a blend comprising or consisting of two, three or more such aldehydes of type (I) and/or (II),as an odoriferous or aroma substance.

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